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GMP Compliance Consultation for Pharmaceutical Industries Worldwide
Consultation for Pharmaceutical,Chemical and Medical Device Industries Worlwide
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About Harpaz Consulting Services

Management
  Daniel Harpaz, MSCHE, MBA, Ph.D., President, has over 30 years experience developing, processing, controlling pharmaceutical and chemical products. He provides his worldwide clients, manufacturers of dosage forms and/or Active Pharmaceutical Ingredients, with extensive hands-on experience including: the Development of Validation Programs, GMP Compliance, Auditing, Vendor Certification, SOP Development, Training, CMC and DMF Preparations.

  He managed Process Development at Merck Sharp and Dohme, Abic Pharmaceuticals and USV Laboratories. He directed Technical Services departments at Revlon Health Care Group (Armour, USV Laboratories, and Norcliff Thayer) and The Mennen Company. Prior to forming HCS in 1993, he was Vice President of R&D at Del Laboratories, where he was responsible for Quality Control, Regulatory Affairs and Product and Process Development departments.

  Dr. Harpaz holds a B.S. and M.S. in Chemical Engineering, MBA in Systems Management and a Ph.D. in Industrial Pharmacy. He publishes and lectures on GMP and Validation issues for APIs, and for Dosage Forms. He is the co-editor of the book titled Validation of APIs, Second Edition published by IHS.

Harpaz Consulting Services' client list includes:
Pfizer Inc, NJ Glaxo, UK
Johnson & Johnson, Consumer products, NJ Natural Pharmaceuticals, Inc., MA
Brantford Chemicals, Canada Warner Lambert, NJ
Amide Pharmaceuticals, NJ Fine Chemicals, South Africa
Sun Pharmaceutical Industries, India Union Carbide, NJ
Searle-Monsanto, PR AlliedSignal, NJ
Cell Therapeutics, Inc., WA MD Pharmaceutical, Inc.,CA
Medeva Americas, Inc., NY IPCA Laboratories, India
Elan, NJ BioWhitaker, MD
Cambrex, NJ Teva, Chemical Division, Israel
Tyco Health Care, MO  
 
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