Friday May 18, 2012
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Date
Time
Event
May 17, 2012
1:00 PM ET
LEAN Approaches to Development of HPLC Methods for Drug Products
May 24, 2012
1:00 PM ET
Equipment Qualification as a Foundation for Process Validation
May 25, 2012
1:00 PM ET
Designing Clinical Trials for Medical Devices
May 30, 2012
10:00 AM ET
Records and Information Management - Intellectual Property
Jun 5, 2012
1:00 PM ET
Establishment Licensing for Pharmaceuticals - Request more information
Jun 6, 2012
1:00 PM ET
Drug Product Stability and Shelf-Life - Request more information
Jun 7, 2012
1:00 PM ET
Validation of Lyophilization - Request more information
Jun 11, 2012
1:00 PM ET
The recent ICH Q11 Guideline - Request more information
Jun 12, 2012
1:00 PM ET
Dietary Supplement current Good Manufacturing Practices(cGMPs) - Request more information
Jun 13, 2012
1:00 PM ET
Auditing the QC Microbiology Laboratory for FDA Compliance - Request more information
Jun 13, 2012
10:00 AM ET
Records and Information Fundamentals For Regulatory Compliance
Jun 19, 2012
1:00 PM ET
Reviewing your Cleaning Program Prior to a Regulatory Inspection
Jun 27, 2012
10:00 AM ET
Long Term Preservation Strategies For Essential Records
July 9, 2012
1:00 PM ET
Basic Concepts for Performing Equipment
Installation Qualification (IQ), Equipment Qualification (OQ), and Performance Qualification (PQ)
July 10, 2012
1:00 PM ET
How Best to Prepare for a GMP Compliance Audit
Sep. 10, 2012
1:00 PM ET
Cleaning for Dietary Supplements/Nutraceuticals Facilities
Sep. 13, 2012
10:00 AM ET
Analytical Standards: The Ultimate Control
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Friday May 18, 2012 Friday May 18, 2012
