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

BAXTER HEALTHCARE CORP RECEIVES SINGLE WARNING LETTER FOR TWO LOCATIONS (05/31/13)

June 17, 2013 By Barry Friedman Leave a Comment

TOTAL MANAGEMENT COLLAPSE OF TERMINAL STERILIZATION OCCURS AT THE MARION, NC FACILITY BASED UPON FDA FINDINGS The FDA recently audited two Baxter Healthcare facilities to include Marion, NC (November 7 to 16,2012) , and Jayuya, Puerto Rico (March 13, 2013 to April 19, 2013).  Their Investigators identified significant violations of current good manufacturing … [Read more...]

FDA CDER Most Frequent Form FDA 483 Observations Fiscal Year 2012

April 24, 2013 By Barry Friedman Leave a Comment

COMMENT Each year CDER summarizes the number of significant Observations obtained from Form FDA 483s.  Enclosed are the "top fifteen" Observations.  The Observations within the top fifteen usually do not change — although their frequency and ranking may vary. Please note that the frequencies of various Observations have … [Read more...]

JUBILANT HOLLISTERSTIER RECEIVES WARNING LETTER (2/13/13)

March 29, 2013 By Barry Friedman Leave a Comment

ASEPTIC FILLING FACILITY RECEIVES SIGNIFICANT OBSERVATIONS Jubilant HollisterStier located in Kirkland, Quebec, Canada was audited by the FDA on March 19-26, 2012.  Following the receipt of the Form FDA 483, the Company responded on April 13, 2012 to the Observations and subsequently on May 1, June 1, and August 9, 2012.  The various violations caused the drug products to be … [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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