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Barry A. Friedman, PhD LLC

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

FDA’S CDER LISTING OF TOP EIGHTEEN OBSERVATIONS FOR 2013

March 20, 2014 By Barry Friedman Leave a Comment

TOP FOUR OBSERVATIONS INCREASE SIGNIFICANTLY OVER 2012 Each fiscal year the FDA issues the various FDA 483 Observations from the various Centers to include CBER, CDER, CDRH, etc.  This Blog focuses only upon those issued by Center for Drug Evaluation and Research (CDER) and will concentrate upon those found within 21 CFR Part 211.  Interestingly, while … [Read more...]

FDA’S CDER SUMMARIZES TOP TEN 483 OBSERVATIONS AT PDA/FDA MEETING IN BALTIMORE (9/12)

September 16, 2012 By Barry Friedman 2 Comments

COMMENT Each year CDER summarizes the number of significant Observations obtained from Form FDA 483s.  At this year's PDA/FDA meetings which were held in Baltimore, MD, the FDA presented the totals calendar year to date.  The Observations within the top ten usually do not change --- although their frequency may vary.  Where a specific section is indicated, the Title indicates … [Read more...]

BEN VENUE RECEIVES YET ANOTHER FORM FDA 483 (12/2/11)

December 6, 2011 By Barry Friedman Leave a Comment

TWELVE PAGE, TEN ITEM 483 COMPLEMENTS 483 ISSUED EARLIER IN 2011 Ben Venue Laboratories received a second audit by four FDA investigators from Nov 7 thru Dec 2, 2011 and received a twelve page Form FDA 483 with ten Observations.  While several of the Observations were similar to those previously received in the May 2011 audit, new Observations were also noted as part of the … [Read more...]

BEN VENUE LABORATORIES RECEIVES FORM FDA 483 FOR ASEPTIC PROCESSING ISSUES (5/25/11)

October 27, 2011 By Barry Friedman Leave a Comment

JUST RELEASED 48 OBSERVATIONS MAY BECOME A PRIMER TO COMPLEMENT FDA 2004 ASEPTIC PROCESSING GUIDANCE The FDA released on Friday, October 14, 2011  a total of 48  Observations within a 33 page Form FDA 483 to Ben Venue Laboratories, Inc., Bedford, OH following an inspection of their facilities from May 2 -25, 2011.  This should become a "must read" primer and complement to FDA's … [Read more...]

CDER MOST FREQUENTLY CITED DRUG OBSERVATIONS – FISCAL YEAR 2010

June 27, 2011 By Barry Friedman Leave a Comment

CDER NAMES THESE TEN (21 CFR 211) Comment The following represent those most frequent Observations that CDER posted for fiscal year 2010 based on a total of 646 FDA Form 483.  REFERENCE              … [Read more...]

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FREQUENTLY ASKED QUESTIONS:

FDA Form 483 Frequently Asked Questions

USP General Chapter

USP General Chapter 62, Part II

TOP OBSERVATIONS:

FDA’s CDER LISTING OF TOP NINETEEN OBSERVATIONS FOR 2014

FDA CDER Most Frequent Form FDA 483 Observations Fiscal Year 2012

CDER MOST FREQUENTLY CITED DRUG OBSERVATIONS – FISCAL YEAR 2010

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