R&Q's Blog

Medical device industry news and trends - and the resources to understand and act on them.

 

Guidance document clean-up! - CDER

I read an interesting article on the RAPS website this morning about a new initiative set by the FDA to clean-up certain guidance documents. This means finalizing draft guidance documents, withdrawing or updating/revising outdated guidance documents. This initiative is taking place in the Center for Drug Evaluation and Research (CDER) department.

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