Clients

Identification, Correction and Prevention of Human Errors in GMP Manufacturing and Laboratory Processes

LIVE, INTERACTIVE WEBINAR
Date: Tuesday June 18, 2012 Time: 1:00 - 3:00 PM ET
Detailed Information>>>

Preparing for FDA GMP Inspections; Successful Strategies and Logistics

LIVE, INTERACTIVE WEBINAR
Date: Tuesday July 9, 2013 Time: 1:00 - 3:00 PM ET
Detailed Information>>>

Lot Disposition; Clinical vs. Commercial – FDA, EMA, ICH Regulations & Guidance

LIVE, INTERACTIVE WEBINAR
Date: Wednesday July 10, 2013 Time: 1:00 - 3:00 PM ET
Detailed Information>>>

Biosimilars; The New 2013 FDA Draft Guidance, European Requirements & Biosimilar Biologic's Pathway to Success

LIVE, INTERACTIVE WEBINAR
Date: Wednesday July 17, 2013 Time: 1:00 - 3:00 PM ET
Detailed Information>>>

Cold Chain Management - The Latest Regulatory Requirements for Product Distribution in the USA, Canada, and the EU; Detailed Analysis of the Recently Issued 2011 EU GDP Guidance

LIVE, INTERACTIVE WEBINAR
Date: Thursday July 25, 2013 Time: 1:00 - 3:00 PM ET
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Meeting the Regulatory GMP Requirements During Clinical Manufacturing - The Difference in Applying the GMPs in the Clinical vs. Commercial Manufacturing

LIVE, INTERACTIVE WEBINAR
Date: Tuesday October 8, 2013 Time: 1:00 - 3:00 PM ET
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Batch Record Review Process - 2013 Requirements in an Evolving Regulatory, Operational and Technological Landscape in the US, EU & Canada

MULTI PART LIVE TRAINING PROGRAM
Part 1: Thursday October 10, 2013
Part 2: Thursday October 24, 2013
Time: 1:00 - 3:00 PM ET
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Product Stability and Expiry Dating - Integrating the Program into the Product Life Cycle from Inception through Commercial Operations and Latest FDA, EMA & ICH Regulations & Guidance

LIVE, INTERACTIVE WEBINAR
Date: Tuesday October 22, 2013 Time: 1:00 - 3:00 PM ET
Detailed Information>>>