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

HAMELN PHARMACEUTICALS, HAMELN, GERMANY RECEIVES WARNING LETTER (12/17/12)

January 22, 2013 By Barry Friedman Leave a Comment

IN-HOUSE STERILITY TESTING METHOD NOT EQUIVALENT TO USP<71> During the time frame of June 4 - 14, 2012, the Hameln facility was audited by the FDA.  Following the audit, the firm responded on July 4, August 2 and 31, and September 8, 2012.  Even with all of these responses, the FDA found that the firm lacked sufficient corrective actions. For … [Read more...]

TOP POSTINGS FROM THE BLOG OF BARRY A. FRIEDMAN, Ph.D., LLC — 2012

January 6, 2013 By Barry Friedman Leave a Comment

Often the question is asked "what were your top postings during the previous year.  This is an intriguing question since I don't know myself until I review the postings at the end of each year.  With an accumulation of over 70,000 views, it is of interest to determine what you, the viewers, deemed to be the most important. I have now sorted through the … [Read more...]

NEW ENGLAND COMPOUNDING CENTER (NECC) DECLARES BANKRUPTCY

December 27, 2012 By Barry Friedman Leave a Comment

The CBS Evening News (12/21, story 9, 0:25, Pelley) reported "The specialty pharmacy linked to that deadly meningitis outbreak filed for chapter 11 bankruptcy protection today." NBC Nightly News (12/22, story 7, 0:25, Holt) added that the Framingham, Massachusetts-based specialty pharmacy "is facing 130 … [Read more...]

FDA APPROVES RAXIBACUMAB TO TREAT INHALATION ANTHRAX (12/14/12)

December 16, 2012 By Barry Friedman Leave a Comment

FIRST MONOCLONAL APPROVED UNDER FDA'S ANIMAL EFFICACY RULE The U.S. Food and Drug Administration today approved raxibacumab injection to treat inhalational anthrax, a form of the infectious disease caused by breathing in the spores of the bacterium Bacillus anthracis. Raxibacumab also is approved to prevent inhalational anthrax when alternative therapies are not available or … [Read more...]

HEMOFARM A.D., VRSAC, SERBIA, RECEIVES WARNING LETTER (6/20/12) FOR ASEPTIC PROCESSING ISSUES

December 9, 2012 By Barry Friedman Leave a Comment

EXAMINE HOW THE REVISED USP<1116> RELATES TO THESE OBSERVATIONS FIRM IS PLACED UNDER FDA IMPORT ALERT Hemofarm A.D., Vrsac, Serbia recently received a four Observation Warning Letter for unreliable environmental (to include microbiological) monitoring data.  Several of the CGMP violations listed in their letter include … [Read more...]

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FREQUENTLY ASKED QUESTIONS:

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FDA’s CDER LISTING OF TOP NINETEEN OBSERVATIONS FOR 2014

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