Course Description

Granulation, Tabletting and Capsule Technology

August 15-18, 2016
Burlingame, CA

Course Offering 1608-301
Course ID 541

In-Person Course

Who Should Attend?
This broadly based course is intended for all scientists and technologists concerned with the development and processing of tablets, capsules and similar products, and with related drug regulatory affairs.

The material will be presented in such a way as to be of value to a varying level of expertise. This course will especially benefit those in:
  • Quality Assurance
  • Marketing
  • Validation
  • Purchasing
  • R&D
  • Regulatory Affairs
  • Manufacturing/Production
  • Engineering Support

Note: Persons seeking an in-depth treatment of only one or two of the major topics of this broadly based program may wish to consider alternative, more specialized courses offered by CfPA in this area of technology.

RAPS - Regulatory Affairs Professional Society
This course has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's recertification of their Regulatory Affairs Certification (RAC) upon full completion.

Course Description
The main aim of this course is to review the science relating to tabletted and encapsulated pharmaceutical products. The course begins with a consideration of raw material testing and the basic aspects of powder and granulation technology, progresses through formulation of solid dosage forms to manufacturing processes and equipment including scaleup and technology transfer. The program concludes with key aspects of the evaluation of finished products and the regulatory constraints that must be considered at each stage.

Formal sessions of the course are supplemented with informal discussion periods between lecturers and course participants and problem-solving sessions are held on both an open and private basis.

Course Director
Dr. Cecil W. Propst; Director, Scientific Affairs, Team Engineering Services, Kalamazoo MI

Dr. Cecil W. Propst is Director, Scientific Affairs for Team Engineering Service, a formulation, and engineering support firm located in Kalamazoo Mi. He was Director of R&D (Grand Haven site) at SPI Pharma until semi retirement in 2015. He served as Director of Quality Assurance and Technical Services at Fleming and Company, and before that, President of Manufacturing Chemists. His duties included system design, product and process development and regulatory affairs. Previously, he served as cGMP Facilities Director for the University of Maryland at Baltimore, in connection with the University’s SUPAC contract with the FDA. Dr. Propst also served as Director of Technical Development for Stellar Manufacturing; Director of Quality Compliance for SmithKline Beecham; Director, Quality Assurance for Norcliff Thayer (a Revlon Company); and Group Leader/Product Development and Manager/Quality Control for Lewis Howe Company. He also serves as a consultant in the area of product development and process investigations for the chemical, diagnostic, food, engineering and beverage industries.

Venue Information
venue
Embassy Suites San Francisco Airport
150 Anza Boulevard
Burlingame , CA 94010 US
Phone: 650-342-4600
Website: Embassy Suites San Francisco Airport

PLEASE NOTE: Participants must make their own reservations; the cost of hotel accommodation is not included in the course fee. Final hotel information will be emailed to you in your confirmation package approximately 3 weeks prior to the course start date.