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CfPA-The Center for Professional Advancement, New Brunswick, NJ
November 2-3, 2015
Who Should Attend?
The course is designed for individuals engaged in the pharmaceutical Semi-Solid dosage forms. It is intended for individuals who work in formulation development, raw materials selection, drug delivery systems, scale-up and manufacturing process, validation, clinical supply manufacture and quality testing. Such personnel include:
• Semi-solid Formulation Scientists
• Manufacturing supervisors/Engineers/Managers
• Manufacturing Operators/Technicians
• Pilot Plant Operation and Scale-Up
• Regulatory Affairs/Quality Control
• CMC Project/Technology Transfer Staff
• Project Managers/Business Development
• R&D scientists/Technicians Course Description
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Organized by:
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CfPA-The Center for Professional Advancement |
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Invited Speakers:
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| Mukund "Mike" Yelvigi; Founder and Principal, Center for Pharmaceutical Integration, LLC. New Jersey |
Mike Yelvigi is founder & principal at Center for Pharmaceutical Integration LLC, which provides consultation service to the industry in the area of CMC support &Technology Integration and Transfers (mergers & acquisitions). He retired as Sr. Director and Head of CMC Therapeutic Area Management function at Pfizer/Wyeth Inc. NY. He had responsibility for co-ordination of CMC activities related to drug substance synthesis, drug product formulation, analytical development and regulatory filing for several therapeutic areas. He has over thirty years extensive experience in pharmaceutical formulation, process development/scale-up, process validation, manufacturing and pre-approval inspections and has successfully launched several products globally. He obtained his undergraduate degree in Pharmacy from Bombay University and graduate degree from Philadelphia College of Pharmacy.
He is an adjunct Assistant Professor of Pharmaceutics at the School of Pharmacy, University of Mississippi and an active member of AAPS, ISPE, AAiPS, FIP. He was the Chairperson of the AAPS Manufacturing Science & Engineering section and is also an Executive committee member of the Industrial Pharmacy Section of FIP. He is an editorial board member of Pharma Times journal.
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Deadline for Abstracts:
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n/a
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Registration:
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Please click here for registration information.
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E-mail:
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sberg@cfpa.com
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