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Training Course:

Complaint Procedures for Medical Devices

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:

'' Complaint handling systems have come under intense scrutiny by the FDA in recent years. This course will examine the current industry FDA environment and will give you tools for survival. It will provide a step-by-step guide to the setting-up, operation, management and auditing of a complaint system for today¡¯s medical device industry environment.

There will be case studies in which various examples of complaint systems will be presented. Pragmatic, simple, statistical trend methods will be reviewed and attendees will utilize what they learn in a series of workshops.
...''

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:

Gums and Hydrocolloids
Microencapsulation and Particle Coating
Documentation Management and Control
Analytical Methods Validation for FDA Compliance
Drug Product Stability and Shelf-Life
Microbiological Control and Validation
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
Early Stage Clinical Studies for Drugs and Devices
Drug Delivery Technologies
Drug Specifications for APIs and Drug Products
The Quality System
Good Clinical Practices (GCP)
Generic Drug Approvals
Generic Drug Approvals
Good Clinical Practices (GCP)
Quality Audits


Notice: The course description on this page was captured from the Internet as historical reference or submitted by visitors.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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