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Mr. Anisfeld Michael

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Mr. Anisfeld Michael
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  • With over twenty-five years expertise in the healthcare industry, Mr. Anisfeld has held senior management positions in international technology transfer, quality assurance, quality control and production. In the course of his career, he has designed pharmaceutical, medical device and bulk pharmaceutical chemical facilities in seven countries. A member of the faculty of the University of Illinois, where he lectures in pharmaceutical technology, Mr. Anisfeld holds higher degrees in Pharmaceutical Technology (M.Sc.), Management (MSM) and Business Administration (MBA).

Mr. Michael Anisfeld is senior consultant for Globepharm Consulting specializing in GMP/Quality activities for the healthcare manufacturing industries. In his current position he numbers among his clients United Nations Agencies, national regulatory agencies (including the US-FDA) and more than 200 pharmaceutical, medical device, biotechnology and bulk pharmaceutical companies in North America, Europe and Asia.

Mr. Anisfeld has established and directed quality control, quality assurance, production and materials management functions in the industry. He has instituted innovative, cost-effective auditing programs for his clients, ensuring that they pass regulatory inspections the first time.

With over twenty-five years expertise in the healthcare industry, Mr. Anisfeld has held senior management positions in international technology transfer, quality assurance, quality control and production. In the course of his career, he has designed pharmaceutical, medical device and bulk pharmaceutical chemical facilities in seven countries. A member of the faculty of the University of Illinois, where he lectures in pharmaceutical technology, Mr. Anisfeld holds higher degrees in Pharmaceutical Technology (M.Sc.), Management (MSM) and Business Administration (MBA).

An active member of many European and American regulatory and technical associations, he has served on the Board of Directors of the Parenteral Drug Association (PDA) and been chairman of its quality control and aseptic processing task groups. He currently serves on the FIP Task Force on Counterfeit Drugs and other international industry forums. An acclaimed international lecturer on the subject of GMP and quality topics, Mr. Anisfeld is also a prolific author on these subjects. He is the editor and author of many texts, including: International Drug GMPs, International Device GMPs, Guide to FDA Pre-Approval Inspections, Sterile Pharmaceutical Manufacturing, and PDA’s monograph Validation of Aseptic Processing of Liquid Drug Products.

About Globepharm
The rapidly accelerating pace of technological and regulatory change has resulted in the need for industry professionals to constantly review and improve their operations and their skill bases, or face obsolescence.
Globepharm organizes conferences, as well as public and in-house courses worldwide, to keep technologists and management current on developments affecting the industry. Faculty are selected based on their meeting criteria for expertise in their field, and for their proven teaching ability. In all of Globepharm’s courses, the emphasis is on the practical and applied, so that participants can return to their facilities and immediately implement the techniques taught in the Globepharm course. Globepharm currently offers courses worldwide for the biotechnology, active pharmaceutical ingredients, diagnostic, medical device and pharmaceutical manufacturing industries.

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