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Kevin Madagan

Kevin Madagan

ID: 1b83654f-2619-30fb-68c4

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Claimed Record

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Organization: Reed Smith LLP

FDA Issues Draft Guidance Regarding When to Submit a 510(k) for a Change to an Existing Device; Guidance Follows 510(k) Working Group Recommendations

Health Industry Washington Watch · July 28, 2011

FDA Reverses Course on Drug Pedigrees: Pedigrees No Longer Required Back to Manufacturer

Life Sciences Legal Update · July 22, 2011

Reed Smith Health Care Reform Review: The Affordable Care Act – Analysis and Implications for Drug, Device and Biotech Manufacturers

Life Sciences Legal Update · June 24, 2010

Reed Smith Health Care Reform Review: The Affordable Care Act – Analysis and Implications for Drug, Device and Biotech Manufacturers

Health Industry Washington Watch · June 24, 2010

FDA Launches “Bad Ad” Initiative

Health Industry Washington Watch · May 13, 2010

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Practice Areas

Communications, Media & Entertainment

Health Care and Life Sciences

Food, Drug & Agriculture

Technology and AI

Jurisdictions

Publishing Record

Publisher Since 2008

Total Articles 50

Most Recent May 21, 2024

Cite This Author

Kevin Madagan, Reed Smith LLP

LexBlog Author ID:

1b83654f-2619-30fb-68c4

www.lexblog.com/author/kmadagan

Contact

FirmReed Smith LLP

Emailkmadagan@reedsmith.com

BlogsHealth Industry Washington Watch

Life Sciences Legal Update

Technology Law Dispatch

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