Training Course:Complaint Procedures for Medical DevicesSchool/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
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