ISPE Announces Q4 2011 Global Training Event Schedule

ISPE, a global not-for-profit association of 22,000 pharmaceutical professionals who use expert knowledge to create high-quality, cost-effective GMP solutions, announced today that it will offer six training events throughout the fourth quarter of 2011.

These events will collectively contain 19 courses on a wide variety of topics vital to the pharmaceutical industry, such as cGMPs, GAMP®, commissioning and qualification, biopharmaceuticals, critical utilities (HVAC and Water), OSD, PAT, project management and sterile products.

“With end-of-the-year training deadlines approaching, many pharmaceutical professionals are seeking ways to fulfill requirements, or just to expand their skills and gain additional knowledge,” said ISPE President and CEO Bob Best. “Our slate of fourth-quarter training events is designed to offer something relevant to almost every specialty and experience level in the industry.”

As a Member-based organization, ISPE is dedicated to creating first-to-market solutions that help Members and their employers in their work to ensure the safety of the world's supply of medicines. ISPE's training courses are an extension of that philosophy. By offering timely and unparalleled education that drives individual competence through the exploration of practical industry challenges, ISPE fosters expertise that is sought by regulators and new industry influencers world-wide.

The training events and course offerings are:

•19-20 September - Brussels, Belgium
oModern Approaches to Risk-Based C&Q
oManaging the Risk of Cross Contamination

•19-22 September - Indianapolis, Indiana, USA
oGMP Auditing for the Pharmaceutical Industry
oOral Solid Dosage Forms
oPharmaceutical Water Generation
oHVAC for Pharmaceutical Facilities
oFacility Project Management in the Regulated Pharmaceutical Industry
oCleaning Validation Principles
oPharmaceutical Water Storage and Distribution

•6-7 October - Norwood, Massachusetts, USA
oPharmaceutical Water Storage and Distribution
oApplying the GMPs
oProcess Validation in Biotechnology Manufacturing
oBiopharmaceutical Manufacturing Facilities

•24-25 October - Philadelphia, Pennsylvania, USA
oBasic Principles of Computerized Systems Compliance (GAMP5®)

•9-10 November - Grapevine, Texas, USA
oRisk-Based Approach to GxP Process Control Systems
oModern Approaches to Risk-Based C&Q
oManaging the Risk of Cross Contamination

•16-17 November - Brussels, Belgium
oSterile Drug Manufacturing Facilities
oImplementing Process Analytical Technology

Full course descriptions, instructor bios, and registration information can be found here. For press passes to attend these events, please contact ISPE Communications Manager Danielle Hould at dhould@ispe.org or call +1-813-960-2105, ext. 277.
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