published 05/25/12
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published 01/26/12
published 03/12/12
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The objective of this 60-minute webinar is to present an overview of the recently launched certification scheme by the International Pharmaceutical Excipients Council (IPEC). Special emphasis is on how to set up the certification scheme. Also some highlights will be presented how and where companies need to start to successfully introduce this into their manufacturing and quality control structure working along the lines of Good Manufacturing Practices as set out by IPEC.
This webinar will be of most interest to those that have a general interest in the GMP quality aspects of Pharmaceutical non-active ingredients (excipients). More specifically, personnel that are working in or are associated with manufacturing facilities engaged in excipients production and control and interested to learn more about and / or create a quality structure following the guidance for Good Manufacturing Practices as set out by IPEC. Typically, quality, regulatory, manufacturing personnel and general management will take benefit from this webinar presentation.
Dr. Eize de Boer, International Business Development Manager for Systems & Services Certification in the Pharmaceutical sector.Dr. de Boer has a background in chemistry and was working for the Pharmaceutical industry in different roles in Manufacturing and Quality. At SGS he is responsible for the third party auditing program to support quality management in the Pharmaceutical industry.
Register for session 1 08:00 a.m. London09:00 a.m. Paris, Berlin, Madrid, Amsterdam03:00 a.m. New York04:00 p.m. Singapore, Kuala Lumpur
Register for session 2 3:00 p.m. London4:00 p.m. Paris, Berlin, Madrid, Amsterdam10:00 a.m. New York11:00 p.m. Singapore, Kuala Lumpur