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The Fourth Annual Medical Device Regulatory, Reimbursement and Compliance Congress

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The Fourth Annual Medical Device Regulatory, Reimbursement and Compliance Congress is a hybrid event scheduled for November 9-11, 2009, in Washington, DC. It aims to enhance legal and regulatory compliance within the medical device industry by discussing key topics such as national health reform implications, federal and state disclosure initiatives, and best practices in compliance. The congress will feature various sessions led by industry experts and government officials, targeting executives, compliance officers, and legal counsel from medical device firms.

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How to get into medical device regulatory affairs?

An Act to amend the Federal Food, Drug, and Cosmetic Act to provide for the safety and effectiveness of medical devices intended for human use, and for other purposes. The U.S. legislation enacted in 1976 amended the Food, Drug, and Cosmetic Act of 1938 signed by the 32nd President of the United States Franklin D.

What does Congress mean in the pharmaceutical industry?

A medical congress is a large meeting held annually where healthcare providers and developers of medical devices and drugs can come together and exchange research and learnings.

What is medical device regulatory compliance?

Medical device compliance refers to the adherence to regulatory standards and requirements set by governmental and industry bodies for the design, manufacturing, testing, marketing, and distribution of medical devices.

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