Pharmaceutical Technology Transfer
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This course is available as a client site course. Please click here for more information.
Who Should Attend
This course is intended for individuals from:
• Product Development
• Regulatory Affairs
• Quality Assurance
• Analytical Development
• Process Development
• Quality Control
• Package Engineering
• Manufacturing
• Project Management and Planning
Participants will benefit by gaining a better understanding of
the complexities of technology transfer of various dosage
forms in the pharmaceutical industry.
Description
This course will provide a basic understanding of the
technology transfer of analytical methods, quality control
standards, packaging components/operations and various
pharmaceutical dosage forms from R&D to manufacturing.
It is designed to provide an understanding of the issues
affecting the transfer within and outside a company. Topics
will include transfer of technology to/from international sites
as well as to/from third parties. Regulatory requirements
and recommended approaches will be discussed. Speakers
will use practical examples to highlight issues critical to
successful technology transfer. Best practices from several
pharmaceutical companies and contract manufacturers will
be presented and contrasted.
Other Courses of Interest
Biopharmaceutical Process Systems
IQ, OQ, PQ
Mar 13 2012, New Brunswick, NJ
IQ, OQ, PQ
May 14 2012, Amsterdam, The Netherlands
Pharmaceutical Process Development
Apr 23 2012, Amsterdam, The Netherlands
Pharmaceutical Risk Management Tools: Getting the Most Out of ICH Q9
Pilot Plant and Scale-up Studies
Mar 05 2012, Amsterdam, The Netherlands
Pilot Plant and Scale-up Studies
Apr 16 2012, New Brunswick, NJ
Process Plant Start-Up
Apr 23 2012, Amsterdam, The Netherlands
Real World Approaches to PAT and QbD Implementation
Scale-Up and Post Approval Changes Guidelines (SUPAC & API Changes)
Feb 27 2012, New Brunswick, NJ
Scale-Up and Post Approval Changes Guidelines (SUPAC & API Changes)
Jun 11 2012, Amsterdam, The Netherlands
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