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Barry A. Friedman, PhD LLC

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

Guidance for Industry. ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients – Questions and Answers. June 2015

September 9, 2015 By Barry Friedman Leave a Comment

In June 2015 ICH issued a Q & A Guidance document that complements the Guidance for Industry Active Pharmaceutical Ingredients, ICH Q7. 2000. Since 2000, experience with implementing the guidance has created a need for clarification of various sections. ICH Q7 should be applied in combination with the principles laid down for development and manufacturing in … [Read more...]

Cobwebs On Oxygen Analyzer Foil Trans Ox During FDA Inspection

September 6, 2015 By Barry Friedman Leave a Comment

Trans Ox Citations Result in Warning Letter (June 8, 2015) During a November 13, 2014, through November 20, 2014, inspection of Trans Ox pharmaceutical manufacturing facility at 2543 Morningside Drive, Suite A, West Columbia, South Carolina, an investigator from the U.S. Food and Drug Administration (FDA) identified significant violations of current good manufacturing … [Read more...]

Smoke Study Findings Contribute to Mylan Laboratories Warning Letter (8/06/2015)

September 2, 2015 By Barry Friedman Leave a Comment

The following is the second Blog in an on-going series of Blogs obtained from a Warning Letter about Mylan Laboratories, Bangalore, India as well as other Mylan (Agila Specialties Private Ltd.) facilities in India. This second Blog continues the review of the Mylan facilities which were audited February 6-13, 2015 and are located at Plot No. 284-B (19A) Bommasandra Jigani Link … [Read more...]

Mylan Laboratories, India Receives Warning Letter (08/06/2015)

August 28, 2015 By Barry Friedman Leave a Comment

Significant Microbiological Issues were Observed The U.S. Food and Drug Administration (FDA) inspected the following three pharmaceutical manufacturing facilities between August 2014 and February 2015. February 6-13, 2015: Mylan Laboratories Limited OTL, Plot No. 284-B (19A) Bommasandra Jigani Link Road, Ind. Area, Anekal Taluk, Bangalore, 560 105 September 23, 2014 … [Read more...]

A REVIEW OF AN EXTENSIVE ENDOTOXIN WARNING LETTER USING THE NEW FDA “ENDOTOXIN” Q&A AS A BACKDROP

August 27, 2015 By Barry Friedman Leave a Comment

GENERAL The following Blog was initially published on October 1, 2012.  Teva Parenterals Medicines had received a Warning Letter in December 2009 describing extensive issues with Endotoxin. To obtain more information on this subject, please plan to attend a webinar on Wednesday, September 9 sponsored by Tungsten Shield and  COMMENT In … [Read more...]

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