PUBLISHED


UNITED STATES COURT OF APPEALS
             FOR THE FOURTH CIRCUIT


UNITED STATES OF AMERICA, STATE        
OF DELAWARE, COMMONWEALTH OF
VIRGINIA, STATE OF CALIFORNIA,
STATE OF HAWAII, STATE OF
NEVADA, STATE OF TENNESSEE,
STATE OF ILLINOIS, STATE OF NEW
HAMPSHIRE, DISTRICT OF COLUMBIA,
STATE OF FLORIDA, STATE OF
MASSACHUSETTS, STATE OF TEXAS,
STATE OF LOUISIANA ex rel. MARK
RADCLIFFE,                                No. 09-1202
                Plaintiff-Appellant,
                 v.
PURDUE PHARMA L.P.; PURDUE
PHARMA, INCORPORATED,
             Defendants-Appellees.


UNITED STATES OF AMERICA,
                  Amicus Curiae.
                                       
2               UNITED STATES v. PURDUE PHARMA


UNITED STATES OF AMERICA, STATE         
OF DELAWARE, COMMONWEALTH OF
VIRGINIA, STATE OF CALIFORNIA,
STATE OF HAWAII, STATE OF
NEVADA, STATE OF TENNESSEE,
STATE OF ILLINOIS, STATE OF NEW
HAMPSHIRE, DISTRICT OF COLUMBIA,
STATE OF FLORIDA, STATE OF
MASSACHUSETTS, STATE OF TEXAS,
STATE OF LOUISIANA ex rel. MARK
RADCLIFFE,                                  No. 09-1244
                  Plaintiff-Appellee,
                 v.
PURDUE PHARMA L.P.; PURDUE
PHARMA, INCORPORATED,
            Defendants-Appellants.


UNITED STATES OF AMERICA,
                  Amicus Curiae.
                                        
        Appeals from the United States District Court
      for the Western District of Virginia, at Abingdon.
             James P. Jones, Chief District Judge.
                   (1:05-cv-00089-jpj-pms)

                  Argued: January 27, 2010

                  Decided: March 24, 2010

    Before TRAXLER, Chief Judge, AGEE, Circuit Judge,
    and Catherine C. BLAKE, United States District Judge
      for the District of Maryland, sitting by designation.
               UNITED STATES v. PURDUE PHARMA                3
Affirmed by published opinion. Judge Agee wrote the opin-
ion, in which Chief Judge Traxler and Judge Blake joined.


                         COUNSEL

ARGUED: Mark Tucker Hurt, Abingdon, Virginia, for
Appellant/Cross-Appellee. Jennifer O’Connor, WILMER-
HALE, Washington, D.C., for Appellees/Cross-Appellants.
Henry Charles Whitaker, UNITED STATES DEPARTMENT
OF JUSTICE, Washington, D.C., for Amicus Curiae. ON
BRIEF: Paul Wakefield Roop, II, ROOP LAW OFFICE, LC,
Beckley, West Virginia, for Appellant/Cross-Appellee. How-
ard M. Shapiro, Kimberly A. Parker, Christopher E. Babbitt,
Robert A. Mays, WILMERHALE, Washington, D.C., for
Appellees/Cross-Appellants. Tony West, Assistant Attorney
General, Beth S. Brinkmann, Deputy Assistant Attorney Gen-
eral, Michael S. Raab, Civil Division, UNITED STATES
DEPARTMENT OF JUSTICE, Washington, D.C., for
Amicus Curiae.


                         OPINION

AGEE, Circuit Judge:

   The plaintiff-relator, Mark Radcliffe ("Radcliffe"), filed a
qui tam suit in the United States District Court for the West-
ern District of Virginia alleging that his former employer,
Purdue Pharma, L.P. ("Purdue"), defrauded the government
by marketing its pain-relief drug, OxyContin, as a cheaper
alternative to the drug it replaced, MS Contin, which was also
manufactured by Purdue. Radcliffe alleged that Purdue,
through its sales agents and marketing materials, falsely
claimed to physicians that OxyContin was less expensive than
its predecessor, MS Contin, because the "2:1 equianalgesic
ratio between OxyContin and MS Contin . . . ma[de] Oxy-
4                 UNITED STATES v. PURDUE PHARMA
Contin twice as potent and, as a result, cheaper per dose than
MS Contin." J.A. 438. Radcliffe’s suit alleged violations of
the federal False Claims Act, 31 U.S.C. §§ 3729-3733
("FCA"), as well as violations under various analogous state
statutes.1

   While the complaint was under seal pursuant to the proce-
dures outlined in the FCA, Radcliffe filed three separate
amended complaints before serving the Third Amended Com-
plaint on Purdue. Purdue then moved to dismiss on three
grounds: (1) bar and release, (2) the public disclosure bar, and
(3) the failure to satisfy Federal Rule of Civil Procedure 9(b),
which requires that allegations of fraud be pled with particu-
larity. The district court allowed limited discovery on the bar
and release issue but subsequently ruled that a release Rad-
cliffe gave Purdue was ineffective as a ground upon which to
grant Purdue’s motion to dismiss. The district court did, how-
ever, grant the motion to dismiss based on Radcliffe’s failure
to satisfy the pleading requirements of Rule 9(b). Radcliffe
was given 30 days to amend his Complaint and he timely filed
    1
    Congress enacted the [FCA] "during the Civil War in response to over-
charges and other abuses by defense contractors, . . . [with the expectation
that it] would help the government uncover fraud and abuse by unleashing
a posse of ad hoc deputies to uncover and prosecute frauds against the
government." United States ex rel. Wilson v. Graham County Soil &
Water Conservation Dist., 

, 298 (4th Cir. 2008) (quoting
Harrison v. Westinghouse Savannah River Co., 

, 784 (4th
Cir. 1999)). "The FCA imposes civil liability (including treble damages
and a fine of up to $10,000) on persons who knowingly submit false
claims to the government for payment or conspire to use false claims to
obtain payment from the government." 

(citing 31 U.S.C.A.
§ 3729 (West 2003 & Supp. 2007)).
   Private persons, known as "relators", may file FCA suits on the govern-
ment’s behalf. 

see 31 U.S.C. § 3730. Such suits are referred to
as "qui tam" actions. Id.; see Vermont Agency of Natural Res. v. United
States ex rel. Stevens, 

, 768 n. 1 (2000) ("Qui tam is short for
the Latin phrase qui tam pro domino rege quam pro se ipso in hac parte
sequitur, which means ‘who pursues this action on our Lord the King’s
behalf as well as his own.’").
                  UNITED STATES v. PURDUE PHARMA                          5
a Fourth Amended Complaint. Purdue again moved to dismiss
and the district court again granted the motion for failure to
satisfy the strict pleading requirements of Rule 9(b). The dis-
trict court also dismissed the state law claims for failing to
plead fraud with particularity and denied Radcliffe leave to
file a Fifth Amended Complaint.

   Radcliffe now appeals the district court’s grant of the
motion to dismiss and the denial of leave to amend. Purdue
cross-appeals, asserting that the district court erred in refusing
to enforce the "Agreement and General Release" Radcliffe
signed on August 1, 2005 ("the Release"), prior to filing the
qui tam suit. For the reasons that follow, we agree with Pur-
due that the district court erred in refusing to enforce the
Release.2

             I. Background and Proceedings Below

  A.    Radcliffe’s Communications with Purdue and the
        Government

   The district court determined that between 1996 and 2005
Radcliffe, on behalf of Purdue, marketed "OxyContin to indi-
vidual physicians and became familiar with Purdue’s market-
ing claims about OxyContin’s relative cost and potency,
including the claim that there is a 2:1 equianalgesic ratio
between OxyContin and MS Contin." United States ex rel.
Radcliffe v. Purdue Pharma L.P., 

, 774
(W.D. Va. 2008). During this period, Radcliffe was employed
by Purdue as a district sales manager, directly marketing Pur-
due products like OxyContin to physicians. The district court
found that some physicians were skeptical of the claimed 2:1
ratio, but Radcliffe’s supervisor reassured Radcliffe that it
was correct. 

assurances, Radcliffe sought
  2
    Because the Release is a complete bar to Radcliffe’s claims, there is no
need to address Radcliffe’s arguments on the Rule 9(b) dismissal nor the
district court’s denial of leave to amend.
6                 UNITED STATES v. PURDUE PHARMA
independent legal advice in 2004 about the OxyContin claims.

2005, using the alias "John Femaledeer," Rad-
cliffe sent an email to a Purdue director and to Purdue’s Gen-
eral Counsel offering to settle a "‘whistleblower’ suit against
Purdue for fraud based on ‘deceptive pharmacology’". In a
subsequent email "John Femaledeer" (Radcliffe) sought to
"settle" his qui tam claims with Purdue if the company would
invest $40 million in his business startup project. Purdue
rejected the offer.

   Around that same time Radcliffe anonymously contacted
an Assistant United States Attorney for the Western District
of Virginia to determine whether there was any interest in a
claim against Purdue, but did not reveal the particulars of his
claims during those discussions. 

. The district court determined it was "undisputed that
Radcliffe did not disclose the nature of his qui tam allegations
to the government prior to the filing of his Complaint" on
September 27, 2005. 

    B.   The Government’s Investigation of Purdue

   The government had been investigating Purdue prior to the
filing of Radcliffe’s suit. According to a declaration executed
by an Assistant United States Attorney, "one area of investi-
gation concern[ed] whether Purdue falsely marketed OxyCon-
tin as being twice as potent as morphine and, accordingly, less
    3
    Radcliffe’s theory of liability under the FCA is that Purdue defrauded
the government by misleading physicians about the potency and cost-
savings of OxyContin. Purdue’s alleged fraudulent marketing, in turn,
caused physicians to prescribe OxyContin to patients when MS Contin
would have sufficed. Because MS Contin was actually cheaper, Radcliffe
asserts that each time Medicare, Medicaid or another government program
(Veterans’ benefits for example) paid for a prescription of the higher
priced OxyContin induced by Purdue’s fraudulent marketing, the govern-
ment paid a "false claim" subject to the FCA.
                UNITED STATES v. PURDUE PHARMA                   7
expensive than MSContin." 

In the same declara-
tion, the Assistant United States Attorney stated that "the 2:1
comparison of OxyContin to MSContin [sic] [wa]s one of the
areas under investigation." 

2002 and contin-
uing for the next several years, the government sought mil-
lions of documents from Purdue and conducted hundreds of
interviews, some of which pertained to the relative potency
and cost of OxyContin and MS Contin." 

24, 2005, an attorney representing several Purdue
employees spoke with a lawyer from the Department of Jus-
tice regarding topics to be discussed during those employees’
grand jury testimony. 

Department attorney
indicated that she intended to (and subsequently did) ask the
employees "about the dispute over the relative potency of
OxyContin and MS Contin, among other topics, explaining
that this related to the marketing and cost implications of the
relative potencies." 

same time, the govern-
ment began drafting a subpoena that "included requests for all
documents discussing relative analgesic potency or safety of
OxyContin and MS Contin." 

under seal
also reflect that prior to the filing of Radcliffe’s suit, the gov-
ernment had made an additional request for the identity of
"the author and source of different versions of a document . . .
already in the government’s possession" that questioned the
2:1 ratio between MS Contin and OxyContin. 

.

   The government’s investigation of Purdue’s marketing
claims continued after Radcliffe’s execution of the Release.
Indeed, on August 2, 2005, the day after Radcliffe signed the
Release, the government subpoenaed Radcliffe to testify
before the grand jury. 

In September 2005, the
Department of Justice provided Purdue’s counsel with elec-
tronic search terms designed to identify documents pertaining
8                  UNITED STATES v. PURDUE PHARMA
to the potency/cost issue. 

his qui tam suit
on September 27, 2005.4

  On May 7, 2007, the government filed a notice that it
would not intervene in the qui tam suit filed by Radcliffe.
Two days later,

        the government filed a criminal information against
        a related Purdue entity and several Purdue execu-
        tives, along with executed plea agreements for all the
        criminal defendants. Although the criminal charges
        did relate to the misbranding of OxyContin, these
        charges focused on Purdue’s marketing of OxyCon-
        tin as "less addictive, less subject to abuse and diver-
        sion, and less likely to cause tolerance and
        withdrawal than other pain medications."

¶ 20, United States v. Purdue Fred-
erick Co., No 1:07-CR-00029 (W.D. Va.)). The misbranding
charges did not pertain to the 2:1 ratio and although the plea
agreements settled certain civil claims by the government,
they did not address the claims made in the qui tam suit. Rad-

.

    C.    Execution of the Release

   In late June 2005, as part of a workforce restructuring that
substantially reduced Purdue’s sales force, Radcliffe was
offered the option of transferring to a new position or accept-
ing a severance package. Radcliffe opted to leave Purdue and,
in exchange for his execution of the Release, he was given an
enhanced benefits package to which he would not otherwise
    4
    On December 5, 2005, the government filed a motion to stay Rad-
cliffe’s qui tam suit, arguing, inter alia, that allowing the suit to move for-
ward would reveal, publicly, a portion of the grand jury’s investigation. 

court granted the stay and the government’s investigation con-
tinued.
               UNITED STATES v. PURDUE PHARMA                 9
have been entitled, including more than $40,000 in salary
payments. The Release, signed by Radcliffe on August 1,
2005, included the following relevant provisions:

    4. (a) Employee . . . knowingly and voluntarily
    releases and forever discharges [Purdue] of and from
    any and all liability to Employee for actions or
    causes of action, suits, claims, charges, complaints,
    contracts (whether oral or written, express or implied
    from any source), and promises, whatsoever, in law
    or equity, which, Employee . . . ever had, may now
    have or hereafter can, shall or may have against
    [Purdue] as of the date of the execution of this
    Agreement, including all unknown, undisclosed and
    unanticipated losses, wrongs, injuries, debts, claim
    or damages to [Ratcliffe], for, upon, or by reason of
    any matter, cause or thing whatsoever.

    5. To the maximum extent permitted by law,
    Employee agrees that Employee will not seek and
    waives any right to accept any relief or award from
    any charge or action against [Purdue] before any fed-
    eral, state, or local administrative agency or federal,
    state or local court whether filed by Employee or on
    Employee’s behalf with respect to any claim or right
    covered by paragraph 4.

    16. THE PARTIES HAVE READ AND FULLY
    CONSIDERED THE AGREEMENT AND ARE
    MUTUALLY DESIROUS OF ENTERING INTO
    SUCH AGREEMENT. THE TERMS OF THIS
    AGREEMENT ARE THE PRODUCT OF
    MUTUAL NEGOTIATION AND COMPROMISE
    BETWEEN EMPLOYEE AND THE COMPANY.
    EMPLOYEE         ACKNOWLEDGES     THAT
    EMPLOYEE (i) HAS HAD AT LEAST FORTY-
    FIVE (45) DAYS TO CONSIDER THIS AGREE-
    MENT . . . (ii) HAS CAREFULLY READ THE
10              UNITED STATES v. PURDUE PHARMA
     AGREEMENT AND THE DISCLOSURE STATE-
     MENT IN THEIR ENTIRETY; (iii) HAS BEEN
     ADVISED IN WRITING TO CONSULT WITH AN
     ATTORNEY PRIOR TO EXECUTION OF THIS
     AGREEMENT; . . . (v) HAS DISCUSSED IT
     WITH INDEPENDENT LEGAL COUNSEL, OR
     HAS HAD A REASONABLE OPPORTUNITY TO
     DO SO . . . . HAVING ELECTED TO EXECUTE
     THIS AGREEMENT, TO FULFILL THE PROM-
     ISES SET FORTH HEREIN, EMPLOYEE
     FREELY AND KNOWINGLY, AND AFTER DUE
     CONSIDERATION,      ENTERS   INTO   THIS
     AGREEMENT INTENDING TO WAIVE, SETTLE
     AND RELEASE ALL LIABILITY FOR AND
     RECOVERY FROM CLAIMS EMPLOYEE EVER
     HAD, NOW HAS OR MIGHT HAVE AGAINST
     THE COMPANY AS OF THE DATE OF THIS
     AGREEMENT.

J.A. 134-35, 140-41.

  D.   Proceedings in the District Court

   In response to Radcliffe’s Third Amended Complaint, Pur-
due moved to dismiss, arguing in part that the Release was a
complete bar to Radcliffe’s suit. To analyze the enforceability
of the Release, the district court applied "the framework
established by the Ninth Circuit in United States ex rel. Green
v. Northrop Corp., 

(9th Cir. 1995), and United
States ex rel. Hall v. Teledyne Wah Chang Albany, 

(9th Cir. 1997)." 

.

   Characterizing Hall as "an exception to the general rule
against enforcing pre-filing releases to bar subsequent qui tam
suits," 

the district court determined that "the critical
issue [was] the completeness of the government’s knowledge
or the fullness of its investigation." 

the dis-
trict court, "[p]artial knowledge or investigation on the part of
               UNITED STATES v. PURDUE PHARMA                11
the government is insufficient to remove a case from the pur-
view of Green into the exception created by Hall." 

Therefore, even though "the government was aware of the
substance of Radcliffe’s allegations and had begun, but not
completed, its investigation of these allegations as of the date
of the Release," 

Radcliffe’s ability "to supplement
federal enforcement of the FCA by prosecuting these allega-
tions on behalf of the government remains." 

  Accordingly, the district court determined

       [t]he circumstances here fall within the general
    rule articulated in Green that pre-filing releases are
    unenforceable to bar subsequent qui tam actions,
    rather than the Hall exception, because the govern-
    ment had not fully investigated the substance of Rad-
    cliffe’s allegations. Further, the public policy
    concerns raised by Purdue do not alter the relative
    balance of public interests under the Rumery test.
    The general release executed by Radcliffe does not
    bar this action.

   In response to the Fourth Amended Complaint, Purdue
renewed its claim of bar by virtue of the Release. However,
the district court did not address the Release issue because it
again granted Purdue’s motion to dismiss on the grounds that
Radcliffe’s pleading failed under Rule 9(b). Purdue has prop-
erly preserved the issue concerning enforcement of the
Release by filing a timely cross-appeal under Rule 4(a)(3) and
we have jurisdiction pursuant to 28 U.S.C. § 1291.

                   II. Standard of Review

  The district court’s order denied Purdue’s motion to dis-
miss based on the Release. However, Purdue contends, and
Radcliffe apparently agrees, that the district court actually
12              UNITED STATES v. PURDUE PHARMA
granted summary judgment to Radcliffe pursuant to Rule
56(c) on the Release issue.

        It is well settled that district courts may convert a
     Rule 12(b)(6) motion to dismiss into a Rule 56
     motion for summary judgment, allowing them to
     assess whether genuine issues of material fact do
     indeed exist. While it may be preferable for a district
     court to trigger this conversion explicitly, appellate
     courts may take the district court’s consideration of
     matters outside the pleadings to trigger an implicit
     conversion of a Rule 12(b)(6) motion to one under
     Rule 56. The ability of appellate courts to perform
     this conversion sua sponte serves judicial economy
     . . . by sparing the district court an unnecessary
     remand. As the Supreme Court has noted: "It would
     be wasteful to send a case back to a lower court to
     reinstate a decision which it had already made but
     which the appellate court concluded should properly
     be based on another ground within the power of the
     appellate court to formulate."

Bosiger v. U.S. Airways, Inc., 

, 450 (4th Cir.
2007) (internal citations omitted) (quoting SEC v. Chenery
Corp., 

, 88 (1943)); see also Herbert v. Saffell,

, 270 (4th Cir. 1989) (treating Rule 12(b)(6)
motion as motion for summary judgment); George v. Kay,

, 1106 (4th Cir. 1980) ("If it is necessary for the
court to look beyond the pleadings, the 12(b)(6) motion must
be converted into a motion for summary judgment and all par-
ties must be given the opportunity to present materials perti-
nent to such a motion."). In this case the parties provided
evidence and thoroughly briefed the Release issue to the dis-
trict court, which clearly relied on the declarations and other
exhibits presented when determining that the Release did not
bar Radcliffe’s qui tam suit. The parties have also relied on
evidence relevant to the Release issue in their briefs submitted
to this Court. The facts in the record appear to be generally
               UNITED STATES v. PURDUE PHARMA                 13
undisputed and we therefore find it proper to convert Purdue’s
"Rule 12(b)(6) motion to one under Rule 56" and thus con-
sider the district court’s ruling on that basis.

                         III. Analysis

   Upon his departure from Purdue, and in exchange for a
considerable sum of money and other benefits to which he
would not otherwise have been entitled, Radcliffe signed the
Release, an exceedingly broad document. In the Release, Rad-
cliffe agreed to "forever discharge[ ] [Purdue] of and from
any and all liability to Employee for actions or causes of
action, suits, [or] claims . . . whatsoever, in law or equity,
which, Employee . . . ever had, may now have or hereafter
can, shall or may have against [Purdue] as of the date of the
execution of this Agreement . . . ." J.A. 134-35 (emphasis
added). Radcliffe "enter[ed] into this agreement intending to
waive, settle and release all liability for and recovery from
claims [he] ever had, now has or might have against the com-
pany as of the date of this agreement." J.A. 141. Finally, he
"waive[d] any right to accept any relief or award from any
charge or action against [Purdue] before any . . . federal, state
or local court . . . ." J.A. 136.

   The FCA clearly provides that once a qui tam action is
filed, the relator and the defendant may not settle (or at least
may not voluntarily dismiss) the action. 31 U.S.C.
§ 3730(b)(1). The statute does not, however, address whether
the relator’s release of qui tam claims, executed before the fil-
ing of a complaint, is enforceable.

   Purdue asserts that prefiling releases are presumptively
enforceable and that enforcing such agreements in FCA cases
is no different than what is done routinely in other cases
involving "civil rights, antitrust, securities fraud, and RICO
claims" where private enforcement deters conduct detrimental
to the public. Br. of Appellee at 38. According to Purdue,
"private qui tam suits are a hallmark of FCA enforcement
14              UNITED STATES v. PURDUE PHARMA
. . . . The government, and other private individuals, remain
free to prosecute released claims." 

In Purdue’s view,
enforcing the Release in this case upholds a number of impor-
tant public policies, such as encouraging settlement, enforcing
the sanctity of contract, supporting the use of general releases
in the employment context, preventing unjust enrichment, and
discouraging duplicity among contracting parties.

   Radcliffe opposes enforcement of the Release, arguing that
qui tam claims belong to the government, not the relator. In
Radcliffe’s view, he had no individual legally cognizable
claim to release as of August 1, 2005 (the date he signed the
Release) because he only became a partial assignee of the
government’s claim upon filing the complaint, not before. He
further contends that, to be effective, "any release purporting
to settle . . . qui tam claims and bar a qui tam action . . . must
have the express consent of the Attorney General." Response
and Reply Br. of Appellant at 42. Finally, he argues that
enforcing prefiling releases undermines the purposes of the
FCA.

   The government, as amicus curiae, advances a somewhat
middle-ground position in which it asserts that although pre-
filing releases should generally be considered unenforceable,
the district court "should have enforced the Release in this
case." Amicus Br. at 3. This is so, the government argues,
"because the relator’s allegations of fraud were disclosed to
the government independent of the filing of the qui tam action
itself." 

proposes adoption of a rule mak-
ing an "FCA qui tam release[ ] . . . enforceable if the govern-
ment has knowledge of the relator’s allegations of fraud
independent of the filing of the qui tam action itself." Amicus
Br. at 12. This "government knowledge exception," the gov-
ernment argues, comports with the purposes of the FCA
because it vindicates the public interest and simultaneously
promotes "the orderly and efficient private resolution of FCA
cases." Amicus Br. at 14.
                 UNITED STATES v. PURDUE PHARMA                       15
   Radcliffe, Purdue and the government agree that the
enforceability of the Release should be evaluated using the
test applied by the Supreme Court in Town of Newton v. Rum-
ery, 

(1987). In Rumery the Supreme Court reit-
erated the well-established rule that "a promise is
unenforceable if the interest in its enforcement is outweighed
in the circumstances by a public policy harmed by enforce-
ment of the agreement."5 

  A.    Radcliffe’s general release of claims did not require
        the government’s consent to be effective.

   As an initial matter, we do not accept Radcliffe’s assertion
that the Release was ineffective because the Attorney General
did not "sign off" on it. In United States ex rel. Ritchie v.
Lockheed Martin Corp., 

, 1168 (10th Cir.
2009), the United States Court of Appeals for the Tenth Cir-
cuit rejected this same argument. We agree with that court’s
analysis.

  The FCA provides that

      [a] person may bring a civil action for a violation of
      section 3729 for the person and for the United States
      Government. The action shall be brought in the
      name of the Government. The action may be dis-
      missed only if the court and the Attorney General
      give written consent to the dismissal and their rea-
      sons for consenting.
  5
    As the district court correctly noted, we have not interpreted Rumery
in the context of the FCA, though we have stated that "public policy is
implicated only where ‘it is explicit, well defined and dominant, and
ascertainable by reference to the laws and legal precedents and not from
general considerations of supposed public interests.’" Radcliffe, 582 F.
Supp. 2d at 778 n.9 (quoting L & E Corp. v. Days Inns of Am., Inc., 

, 58 (4th Cir. 1993)).
16              UNITED STATES v. PURDUE PHARMA
31 U.S.C.A. § 3730(b)(1) (West 2003); see, e.g., Webster v.
United States, 

at *1 (4th Cir. 2000) (Table)
("with the government’s consent" relator "voluntarily dis-
missed her qui tam action without prejudice"). As the Tenth
Circuit explained:

        [t]he statute itself only mentions the "dismissal" of
     a qui tam action and further requires the consent of
     the court. When there is a release preceding the fil-
     ing of the qui tam action, as in this case, no action
     has been filed, so there is neither an action to dismiss
     nor a judge to consent to the agreement. As a conse-
     quence, the statute only governs the enforceability of
     settlement agreements made after the filing of a qui
     tam claim.

(citing 

).

   Section 3130(b)(1) manifests Congress’ express intent to
prohibit a relator’s unilateral settlement of FCA claims,
absent the government’s consent, once a suit has been filed.
If Congress specifically intended to preclude a relator from
releasing his claims only with the Attorney General’s consent
prior to filing suit, it could have done so, but did not. "We do
not lightly assume that Congress has omitted from its adopted
text requirements that it nonetheless intends to apply . . . ."
Jama v. Immigration and Customs Enforcement, 

, 341 (2005). Thus, the consent of the government is not
a necessary condition precedent to enforcement of an other-
wise valid release where such a release is executed prior to
filing a qui tam action.

  B.   Radcliffe possessed a legally cognizable claim subject
       to the terms of the Release.

   Radcliffe next argues that the plain language of the Release
does not encompass his qui tam claims against Purdue. Spe-
cifically, in paragraph 4 he released Purdue from "all liability
                UNITED STATES v. PURDUE PHARMA                   17
to Employee for . . . claims . . . which Employee . . . ever had,
may now have or hereafter can, shall or may have . . . as of
the date of the execution of this Agreement [August 1, 2005]."
Response and Reply Br. of Appellant at 54. Radcliffe asserts
that as of the date the Release was executed, he had no FCA
claim against Purdue. As support for this proposition, he
relies on the Supreme Court’s statement in Vermont Agency
of Natural Resources v. United States ex rel. Stevens, 

, 773 (2000), that "[t]he FCA can reasonably be
regarded as effecting a partial assignment of the Govern-
ment’s damages claim." In Radcliffe’s view, no such assign-
ment occurred until he filed his complaint under seal with the
district court, which occurred after he signed the Release. We
disagree.

   In Vermont Agency, the Supreme Court explained the three
elements necessary to establish Article III standing. First, a
plaintiff must establish that he suffered an "‘injury in fact’ . . .
that is both ‘concrete’ and ‘actual or imminent, not conjec-
tural or 

(quoting Whitmore v.
Arkansas, 

, 155 (1990)). "Second, he must estab-
lish causation—a ‘fairly . . . trace[able]’ connection between
the alleged injury in fact and the alleged conduct of the defen-
dant." Vermont 

(quoting Simon v.
Eastern Ky. Welfare Rights Org., 

, 41 (1976)).
Finally, "he must demonstrate redressability — a ‘substantial
likelihood’ that the requested relief will remedy the alleged
injury in fact." Vermont 

(quoting

). Noting that in qui tam cases it is the
government and not the relator that has sustained the injury-
in-fact, the Vermont Agency Court held that a relator nonethe-
less possesses Article III standing to bring an FCA claim "be-
cause the [FCA] ‘effect[s] a partial assignment of the
Government’s damages claim’ and that assignment of the
‘United States’ injury in fact suffices to confer standing on
[the relator].’" Sprint Commc’ns Co. v. APCC Servs., Inc.,
___ U.S. ___, 

, 2542 (2008) (quoting Vermont

, 774). Thus, an "adequate basis for
18                 UNITED STATES v. PURDUE PHARMA
the relator’s suit for his bounty is to be found in the doctrine
that the assignee of a claim has standing to assert the injury
in fact suffered by the assignor." Vermont 

(emphasis added).

  In the course of its analysis the Supreme Court further
explained

      that the statute gives the relator himself an interest in
      the lawsuit, and not merely the right to retain a fee
      out of the recovery. Thus, [the statute] provides that
      "[a] person may bring a civil action for a violation
      of section 3729 for the person and for the United
      States Government," § 3730(b).

   According to Radcliffe’s own allegations, the government
suffered an "injury-in-fact" caused by Purdue’s deceptive
marketing of OxyContin’s 2:1 equianalgesic ratio from 1995
to 2005. Thus, once the government suffered an injury (and
Radcliffe became aware of the fraud causing the injury), Rad-
cliffe had a statutory claim, and the necessary legal standing
as partial assignee, to file a qui tam lawsuit.6,7

  In short, he had "an interest in the lawsuit" regardless of
when he opted to vindicate it.8 The fact that Radcliffe chose
  6
     Indeed, Radcliffe’s attempts to settle his claims with Purdue in early
2005, via anonymous emails, indicates that even he understood that he had
an FCA claim well before he signed the Release.
   7
     We note that the elements of causation and redressability are not, in the
context of Racliffe’s allegations, at issue. Clearly, Radcliffe has alleged
that the "cause" of the fraud was Purdue’s marketing practices prior to his
execution of the Release. There is also no doubt that, if violations of the
FCA were eventually proven, monetary damages would be the appropriate
remedy.
   8
     This is not to say that Radcliffe possessed an indefinite, indefeasible
claim. For example, another relator alleging the same fraudulent conduct
                  UNITED STATES v. PURDUE PHARMA                        19
not to file suit until after signing the Release does not negate
the fact that he had the right to file suit beforehand – a right
he waived under the terms of the Release. See 6A C. Wright,
A. Miller, & M. Kane, Federal Practice and Procedure § 1545,
pp. 351-353 (2d ed. 1990) ("[W]hen there has been . . . a par-
tial assignment the assignor and the assignee each retain an
interest in the claim and are both real parties in interest.").
Because Radcliffe possessed a presently enforceable claim at
the time he signed the Release, the plain terms of the Release
encompassed his FCA claims.

  C.    The Government’s Knowledge

  Having determined that Radcliffe’s FCA claims were
encompassed by the terms of the Release and that the Attor-
ney General’s consent to the Release was unnecessary, we
next address, in a Rumery context, whether overriding public
policy considerations nonetheless prevent enforcement of the
Release. We hold that they do not under the facts of this case.

   Most courts considering the enforceability of releases exe-
cuted prior to filing an FCA suit, including the district court
in this case, apply the analytical framework established by the
Ninth Circuit in Green and Hall. See, e.g., 

; United States ex rel. McLean v. County of Santa
Clara, No. C05-01962, 

(N.D. Cal. Apr.
30, 2008); U.S. ex rel. El-Amin v. George Washington Univ.,
No. 95-2000, 

(D.D.C. May 2, 2007);
United States ex rel. Longhi v. Lithium Power Techs., Inc.,

(S.D. Tex. 2007); United States ex rel.
Bahrani v. ConAgra, Inc., 

(D. Colo.
2002).

could have preempted Radcliffe’s suit or Radcliffe could have let the stat-
ute of limitations expire. See 31 U.S.C. § 3730(b)(5) (barring a relator
from bringing "a related action based on the facts underlying [a] pending
action"). The Release, of course, did not prohibit the government or
another relator from pursuing similar claims against Purdue.
20             UNITED STATES v. PURDUE PHARMA
   Green involved an employee who, during his tenure with
a defense contractor, alleged that the company "had ‘double
charged’ the U.S. Air Force for equipment procured for the B-
2 bomber program" and that he had been discharged for rais-
ing the overcharges with company officials. 

. Green filed suit against his former employer, asserting
various state-law claims arising out of his termination. 

eventually reached a settlement and Green signed a
general release resolving "all of the matters which [had]
arisen between them including but not limited to disputes
relating to or arising out of the [lawsuit] and Green’s employ-
ment with and separation from" the company. 

sequently filed a qui tam suit against his former employer
alleging fraudulent conduct subject to the FCA.

   The Ninth Circuit concluded "that enforcing the release . . .
would impair a substantial public interest" and declined to
enforce Green’s release. 

The court deemed it "criti-
cal" to its analysis, however, "that the government only
learned of the allegations of fraud and conducted its investiga-
tion because of the filing of the qui tam complaint." Green, 

After considering additional interests favoring
enforcement, the Green Court determined "that application of
the Rumery[ ] test compels the conclusion that prefiling
releases of qui tam claims, when entered into without the
United States’ knowledge or consent, cannot be enforced to
bar a subsequent qui tam claim." 

    A few years after its decision in Green, the en banc Ninth
Circuit upheld a prefiling release in Hall because, contrary to
the facts in Green, "the government had full knowledge of the
. . . charges and had investigated them before" the relator and
the defendant settled. 

. In Hall, the court
specifically stated that its "refusal to enforce the release in
Green turned on the public interest in learning about claims
of government contractor fraud, and upon the fact that in that
case, the government had not been aware of [the relator’s]
allegations at the time of the settlement release." 

               UNITED STATES v. PURDUE PHARMA                21
But because the government was aware of and had investi-
gated the claims raised by the relator in Hall, "the public
interest in having information brought forward that the gov-
ernment could not otherwise obtain [was] not implicated." 

and Hall, the Ninth Circuit focused
    heavily upon the federal interest in the disclosure of
    fraud. In Green, the government had no knowledge
    of the fraud prior to the filing of the qui tam suit,
    while in Hall the government had already been
    apprised of the allegations due to prior disclosures
    [by the defendant] to a federal agency.

.

   Purdue asserts that independent of any contribution from
Radcliffe, the government’s long-standing investigation of
Purdue’s marketing of OxyContin had specifically come to
include the precise focus of Radcliffe’s suit: "‘whether Purdue
falsely marketed OxyContin as being twice as potent . . . and,
accordingly, less expensive than MSContin [sic] and the accu-
racy of ‘the 2:1 comparison of OxyContin to MSContin
[sic].’" 

. Purdue points out
that not only did the government already have access to the
documents Radcliffe would subsequently attach to his com-
plaint, it also had high-level documents to which Radcliffe
would not have had access as an employee. This is not, there-
fore, a suit based on information that was otherwise unavail-
able to the government. As such, Purdue argues, this is not a
case where public policy precludes enforcement of the
Release.

   Radcliffe argues that for the Hall exception to apply, and
thus for the Release to be enforceable, the government must
(1) have known the substance of the relator’s allegations, and
(2) have fully investigated them by the time a release was
signed. Radcliffe asserts that in refusing to enforce the
Release, the district court correctly focused on the fact that
22             UNITED STATES v. PURDUE PHARMA
the government "had begun, but not completed, its investiga-
tion of these allegations as of the date of the release." 

   The government, as amicus, contends the Release should be
enforced in this case because the government’s knowledge of
a relator’s allegations of fraud vindicates the public interest
goals of the FCA. The government asserts that such a "gov-
ernment knowledge" rule combats any attempt by defendants
to buy relators’ silence and encourages defendants’ disclosure
of fraud and cooperation with investigations. The government
contends that by relying on the fact that it "had not fully
investigated the substance of Radcliffe’s allegations," 

(emphasis added), the district court erroneously applied
the Green/Hall analysis. This is so, the government argues,
because the district court’s reasoning overlooks the primary
purpose of requiring disclosure of fraud allegations, "which is
not to ensure that the government exhaustively investigates
and prosecutes every allegation of fraud, but rather that it has
an adequate opportunity to do so." Amicus Br. at 16. Accord-
ing to the government, giving conclusive weight to the com-
pleteness of its investigation as a condition of enforcing an
FCA release could lead to an inappropriate, time-consuming,
and amorphous inquiry into the government’s internal investi-
gative deliberations and processes. Moreover, such a "com-
pleted investigation rule" contradicts 31 U.S.C. § 3730(b)(2),
which grants the government discretion under the FCA to ini-
tiate or participate in an FCA action without precondition.

   The district court identified several interests to be consid-
ered when enforcing a release of qui tam claims, including
"the public interest in having relators disclose inside informa-
tion of alleged fraud to the government, in having relators
supplement federal enforcement of the FCA by assisting the
government in its investigation and prosecution or prosecut-
ing the claim itself, and in deterring future fraud against the
government." 

. The district
court acknowledged that "the government [learned] of the
               UNITED STATES v. PURDUE PHARMA                23
substance of Radcliffe’s allegations independently and was
interested enough in them to request documents pertaining to
and question various Purdue employees about the relative cost
and potency issue." 

the government’s investi-
gation eventually went "in a different direction" and the final
settlement did not refer to the issue raised by Radcliffe, the
district court ultimately concluded that Radcliffe’s continued
"ability to supplement federal enforcement of the FCA by
prosecuting these allegations" best served the public interest.

court "believe[d] that enforcing the release
under these circumstances would substantially impact impor-
tant public interests associated with the FCA," 

"the fullness of [the government’s] investigation" was a nec-
essary condition precedent to the enforceability of a release.

We disagree.

   The Tenth Circuit recently addressed analogous issues and
determined that "[b]ecause the federal interests served by
enforcing releases signed after disclosure to the federal gov-
ernment outweigh the interests served by not enforcing them,
. . . the releases [were] enforceable." 

. In Ritchie, the defendant self-reported fraud to the gov-
ernment, which conducted its own audit and investigation. 

assisted the government in its investigation but
subsequently settled claims that the company retaliated
against her "because of her whistleblowing activities." 

As a result of the settlement, in which she agreed to
leave the company, the relator signed two releases purporting
to waive "any and all claims [she] might have under federal,
state or local law." 

after signing the second
release she filed a qui tam action against her former employer.

relator’s contentions that "the government
lacked full knowledge of the scope of the fraud at the time she
signed the release," 

the Tenth Circuit affirmed the
district court’s enforcement of the release. In doing so, the
court of appeals determined that "[t]he disclosures to the gov-
24                UNITED STATES v. PURDUE PHARMA
ernment in this case were sufficient to satisfy the public inter-
est in uncovering fraud." 

the court of
appeals, "[e]nforcing releases of qui tam claims only when the
allegations of fraud have been disclosed to the government
before the release . . . has the benefit of encouraging voluntary
disclosure by government contractors." 

"the federal government had not issued its final
audit report when the settlement was reached or the qui tam
suit was filed." 

Accordingly, the circuit court rec-
ognized, as did the district court in this case, that under such
circumstances an interest in having private citizens supple-
ment federal enforcement remains, but "[o]n balance . . . that
interest does not outweigh the federal interests served by
enforcement of settlements following disclosure of fraud alle-
gations to the government, namely the interest in disclosure
of fraud allegations and the interest in encouraging settle-
ment." 

so, in part, because

       [c]ontractors . . . have an interest in settling qui tam
       claims prior to the filing of a lawsuit. If they can set-
       tle qui tam claims only after fraud allegations have
       been disclosed to the government, then contractors
       effectively have an incentive to disclose. On policy
       grounds, then, conditioning the enforceability of
       releases of qui tam claims upon the prior disclosure
       of the fraud allegations to the government promotes
       the federal interest in uncovering fraud against the
       government.

Enforcing prefiling releases also encourages the
settlement of disputes.9 See Crandell v. United States, 703
  9
   The government also points out that if it has knowledge of the alleged
fraud, "[s]uch . . . knowledge . . . reduces the perverse incentive a qui tam
defendant would otherwise have to buy the silence of relators, because that
defendant faces the real threat of an independent government action."
Amicus Br. at 13.
                UNITED STATES v. PURDUE PHARMA                  

, 75 (4th Cir. 1983) ("Public policy, of course, favors
private settlement of disputes.").

   When the government is unaware of potential FCA claims
the public interest favoring the use of qui tam suits to supple-
ment federal enforcement weighs against enforcing prefiling
releases. But when the government is aware of the claims,
prior to suit having been filed, public policies supporting the
private settlement of suits heavily favor enforcement of a pre-
filing release. We therefore agree with the government that
"[t]he proper focus of the inquiry is whether the allegations of
fraud were sufficiently disclosed to the government, not on
whether the government’s investigation was complete."
Amicus Br. at 17. We find that application of this "govern-
ment knowledge" rule meets the balancing analysis required
under Rumery. Thus, we concur with the Tenth Circuit that
when, as in this case, the government was aware, prior to the
filing of the qui tam action, of the fraudulent conduct repre-
sented by the relator’s allegations, the public interest has been
served and the Release should be enforced.

   Accordingly, because the "allegations of fraud were suffi-
ciently disclosed to the government" prior to Radcliffe’s filing
of the qui tam suit, the district court erred in failing to enforce
the Release as a bar to Radcliffe’s claims.

                         IV. Conclusion

   Although we conclude that the district court erred in its
decision not to enforce the Release, we nonetheless affirm the
judgment dismissing Radcliffe’s suit with prejudice. See SEC
v. Chenery Corp., 

, 88 (1943) ("[T]he decision of
a lower court . . . must be affirmed if the result is correct
although the lower court relied upon a wrong ground or gave
a wrong reason . . . . It would be wasteful to send a case back
to a lower court to reinstate a decision which it had already
made but which the appellate court concluded should properly
be based on another ground . . . ." (internal quotation marks
26            UNITED STATES v. PURDUE PHARMA
omitted)); Eisenberg v. Wachovia Bank, N.A., 

,
222 (4th Cir. 2002) (observing that we "can affirm on any
basis fairly supported by the record").

   Accordingly, the judgment of the district court will be
affirmed.

                                               AFFIRMED