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Rottenstein Law Group Reports on Research Paper Concluding FDA’s Medical Device Approval Process Needs Reform.

Rottenstein Law Group Reports on Research Paper Concluding FDA’s Medical Device Approval Process Needs Reform

New York City : NY : USA | Aug 17, 2012 at 9:32 AM PDT SOURCE: PRWEB

Medicine, three Harvard Medical School researchers write that the American and European medical device approval processes are in need of change.

As a law firm representing women who allege they were injured by vaginal mesh products, the Rottenstein Law Group believes the FDA misclassified those products as medical devices that aren’t risky enough to require pre-market human testing.

The Rottenstein Law Group is a New York-based law firm that represents clients nationwide in mass tort actions. The firm’s founder, Rochelle Rottenstein, has more than two decades of experience as a lawyer, and compassionately represents clients in consumer product injury, mass tort, and class action lawsuits.

Contact:

The Rottenstein Law Group, LLP

Rochelle Rottenstein, Esq.

321 W. Street

Suite 511

New York NY 10036

(212) 933-9500 (office phone)

(212) 933-9980 (facsimile)

rochelle(at)rotlaw.com

http://www.rotlaw.com

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