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Training Course:

Documentation Management and Control

School/Trainer:

The Center for Professional Advancement
Amsterdam, Netherlands

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

Course Description:

'' FDA regulations such as Good Manufacturing Practice (GMP) for drugs and medical devices, Good Laboratory Practice (GLP), Good Clinical Practice (GCP), as well as quality system standards like ISO 9000, require that documentation, such as standard operating procedures, plans and various types of records, be in place. These regulations, however, do not provide any guidelines to the industry on how to set up and manage documentation systems. It is, therefore, left to companies to design and set up their own internal documentation systems.

This course provides hands-on methodology and techniques on how to identify what systems require documentary coverage; how to flowchart operations to identify what type of documentation is required; and how to set up, implement and manage the maintenance of such documentation systems to ensure continuous compliance. Types of documentation addressed include: quality manuals, policy manuals, standard operating procedures, work instructions, forms, records, logs, protocols, etc. The course also covers areas related to computer validation documentation, such as validation protocols and 21 CFR Part 11—Electronic Records and Signatures. Emphasis is placed on controls that need to be in place to ensure proper manipulation of documentary systems.

The course consists of lectures, discussions and interactive workshops with classroom presentations.

This basic introductory course is designed for individuals responsible for documentation writing and management in the pharmaceutical and related industries. The course will benefit individuals in a variety of functions such as:

Quality Assurance
Regulatory
Quality Control
Production
R&D
Product Development
Toxicology
Vendors/Suppliers
Clinical Research
CRO¡¯s
...''

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

Phone:+31/20/638.28.06

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: Amsterdam
Houses & Roommates: Amsterdam




Other training courses offered by The Center for Professional Advancement:

Cost Effective Quality-by-Design and Critical-to-Quality Tools for PAT
Conception, Design and Implementation of Plant Safety Systems
Pilot Plant and Scale-up Studies
Atomization, Sprays and Atomizers
Introduction to Skin Aging
LAL Testing: Drugs, Medical Devices and Biopharmaceuticals
Quality Audits
Root Cause Investigation for CAPA
cGMP for Pharmaceutical Production Supervisors
Applied Process Engineering
Equipment Qualification in a Nutshell
Skin Product Development
International Patent Law
Near Infra-Red Spectroscopy
Analytical Methods Validation for FDA Compliance
Excipient GMPs
Sterilization in the Pharmaceutical Industry
Good Laboratory Practices (GLP)
Non-Clinical Drug Safety Evaluation and Drug Development


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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