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FDA Regulatory Compliance for the Pharmaceutical, Biotechnology and Medical Device Arenas

FDA CDER PUBLISHES SEVERAL NEW PRESENTATIONS TO ASSIST WITH REGULATIONS GOVERNING PET DRUG PRODUCTS

February 6, 2012 By Barry Friedman Leave a Comment

DOCUMENTS INCLUDE AN EXTENSIVE SLIDE DECK AND PROPOSED Q & A The FDA has been quite busy since the issuance of the new 21 CFR 212 entitled "Current Good Manufacturing practice for Positron Emission Tomography Drugs" (December 2011) which covers Positron Emission Tomography (PET) Drug Products.  CDER has issued a new Draft Guidance as well as a slide deck from B. Uratani, … [Read more...]

FDA ISSUES — MEDIA GROWTH PROMOTION STUDIES McNEIL-PPC, DELTEX PHARMA, RIBBON PHARMA & CHEMICAL, COLUMBIA PRESBYTERIAN MEDICAL CENTER

April 7, 2011 By Barry Friedman 1 Comment

FDA ISSUES -- MEDIA GROWTH  PROMOTION STUDIES McNEIL-PPC, DELTEX PHARMA, RIBBON PHARMA & CHEMICAL, COLUMBIA PRESBYTERIAN MEDICAL CENTER Comment Comments Regarding Proposed Changes to USP General Chapter <823> Radiopharmaceuticals for Positron Emission Tomography-Compounding were recently made to the USP as they move forward in … [Read more...]

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