View Cart  

‘Informal’ ICH Panel Mulling Revision, Rewrite of Q7 Guideline on API GMPs: FDA Official

TAMPA, Fla. — An informal working group of the International Conference on Harmonisation (ICH) is looking into revising or rewriting the “dated” Q7 standard on good manufacturing practices for active pharmaceutical ingredients (API), an FDA official says.

To View This Article:


Subscribe To Drug Industry Daily