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Training Course:

Microbiological Control and Validation

School/Trainer:

The Center for Professional Advancement
East Brunswick, New Jersey, United States

Course Format: Classroom | E-learning | Virtual Class | Online | On-site | Blended | Self-paced

Course Description:

'' This course will present information on microbiological control in manufacturing, laboratory auditing and sterilization. The course will also cover ISO, EP, BP, USP, AAMI and U.S. FDA documents and guidelines. Validation of sterilization processing will be discussed and case studies will be presented. Environmental monitoring programs will be discussed in depth. Design and testing of product packages for sterility assurance will be covered via case studies. All aspects of microbiological control will be covered. Microbiological testing schemes will be presented and the key aspects of GLP/cGMP will be reviewed. You are invited to bring transparencies of monitoring programs, procedures, flowcharts, etc., for discussions during the case studies on the third day.
...''

Please go to the school's official website for training price and schedule:
http://www.cfpa.com

Phone:(732)238-1600

School Address:

Corporate Office
Box 7077, 44 West Ferris Street
East Brunswick, NJ USA 08816-7077
Phone: (732)238-1600
Fax: (732)238-9113
Email info@cfpa.com

Europe Office
Oudezijds Voorburgwal 316A, 1012 GM
Amsterdam, The Netherlands
Phone +31/20/638.28.06
Fax +31/20/620.21.36
Email amsterdam@cfpa.com



Jobs & Resumes: East Brunswick
Houses & Roommates: East Brunswick




Other training courses offered by The Center for Professional Advancement:

Microencapsulation and Particle Coating
Nanotechnology
ISO 13485, ISO 9001 and QSR Regulations for Medical Device Companies
Project Management
Risk Analysis & Human Factors Engineering
Gums and Hydrocolloids
Microencapsulation and Particle Coating
Documentation Management and Control
Analytical Methods Validation for FDA Compliance
Drug Product Stability and Shelf-Life
Process Validation for the Pharmaceutical and Medical Device Industry
Non-Clinical Drug Safety Evaluation and Drug Development
ADME: Absorption, Distribution, Metabolism and Elimination
Root Cause Investigation for CAPA
Complaint Procedures for Medical Devices
Early Stage Clinical Studies for Drugs and Devices
Drug Delivery Technologies
Drug Specifications for APIs and Drug Products
The Quality System


Notice: The course description on this page was captured from the Internet as historical reference or submitted by visitors. It was archived statically and not updated from day to day.
 


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