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Barry A. Friedman, PhD LLC

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

H and P Industries Lawsuit Ties Tainted Wipes to Twin’s Brain Damage

July 11, 2011 By Barry Friedman 1 Comment

MSNBC Reports On On-Going Rare Bacterial Infection Stumped Experts Until News Of Contaminated Products Surfaced For nearly four years, a bacterial infection that left a Seattle-area newborn with severe brain damage while his twin brother developed normally has remained a medical mystery, traumatizing his family and stumping local and national disease experts. Myles Massey, … [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...]

TOP 15 BACTERIA REPRESENT 50% OF BACTERIAL ISOLATES IDENTIFIED

June 22, 2011 By Barry Friedman Leave a Comment

ACCUGENIX IDENTIFIED WHAT MICROORGANISMS REPRESENT THE OTHER 50% While having knowledge of the most frequently identified bacteria is informative, it is important to note that these Top 15 bacteria identified from manufacturing environments, as cited in the original post, only represent approximately 50% of the microbes that are identified during routine monitoring and … [Read more...]

BEST METHOD TO DETERMINE THE IDENTIFICATION OF A MICROORGANISM

June 2, 2011 By Barry Friedman Leave a Comment

DIFFERENTIATION BETWEEN PHENOTYPIC AND GENOTYPIC IDENTIFICATION MECHANISMS Recently, a Blog was published that identified the fifteen most common bacterial isolates identified by Accugenix, Inc, Newark, DE during 2010.  This Blog created an interest in other related areas to include the best methods to assure a definitive identification of an isolated bacterium. In a poster … [Read more...]

WARNING LETTES ISSUED TO COMPANIES MAKING HAND SANITIZERS

May 24, 2011 By Barry Friedman Leave a Comment

FDA WARNS COMPANIES TO STOP MAKING MRSA CLAIMS FOR OVER-THE -COUNTER PRODUCTS (4/20/2011) Comment The FDA recently sent Warning Letters to the four companies listed below for "making unproven prevention claims". ".... the labeling of some of the firms’ hand sanitizing drug products make claims related to preventing infection from E.coli and/or … [Read more...]

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FREQUENTLY ASKED QUESTIONS:

FDA Form 483 Frequently Asked Questions

USP General Chapter

USP General Chapter 62, Part II

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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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