The Center for Professional Advancement, Amsterdam
5-6 December 2007
Who Should Attend:
This course is intended for individuals fromFormulation Development
Process Development
Regulatory Affairs
Quality Control
Quality Assurance
Package Engineering
Analytical Development
Manufacturing Participants will benefit by gaining a better understanding of the complexities of technology transfer 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.
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