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OIG Compliance Program Guidance for Pharmaceutical ManufacturersDeveloping the Compliance Program Guidance for Pharmaceutical ManufacturersOn June 11, 2001, the OIG published a solicitation notice seeking information and recommendations for developing compliance program guidance for the pharmaceutical industry (66 FR 31246). In response to that solicitation notice, the OIG received eight comments from various outside sources. We carefully considered those comments, as well as previous OIG publications, such as other compliance program guidances and Special Fraud Alerts. In addition, we have taken into account past and ongoing fraud investigations conducted by the OIG’s Office of Investigations and the Department of Justice, and have consulted with the Centers for Medicare and Medicaid Services (CMS) (formerly known as the Health Care Financing Administration). In an effort to ensure that all parties had a reasonable opportunity to provide input into a final product, draft compliance program guidance for the pharmaceutical industry was published in the Federal Register on October 3, 2002 (67 FR 62057) for further comments and recommendations. ← Background | Main | Elements for an Effective Compliance Program →Toll Free: 800-FRAUD 04 Nolan Law Firm - 435 North Andrews Avenue, Suite 401, Ft Lauderdale, FL 33301 Home | About Nolan Law Firm | Frequently Asked Questions | Whistleblower Resources Overviews: The hiring of a lawyer is an important decision that should not be based solely on advertisements. Before you decide, ask us to send you free written information about our qualifications and experience. Disclaimer | Copyright © 2006 Nolan Law Firm All Rights Reserved. |