Training Course:cGMP Auditing - Strategies for ComplianceSchool/Trainer:The Center for Professional Advancement
New Brunswick, United States
Course Format: Classroom | E-learning | Virtual Class | Online | On-site | Blended | Self-paced
Course Description:
'' This practical, introductory course was designed to provide a mechanism for those interested in understanding the basic requirements for auditing in the pharmaceutical and related industries.
The course presents an introduction to the evolutionary process of FDA regulations and describes in detail the latest FDA initiatives in the inspection process. It provides a road map for auditors in setting up a cGMP audit trail from beginning to end. Specific compliance aspects like change control, outsourcing, and validation will be presented as they pertain to the audit function. The course will consist of lectures, interactive discussions and a hands-on workshop.
Newly assigned auditors or those who expect to be involved in auditing in the near future, will find this course beneficial. Those individuals who expect their departments, groups or functions to be audited will also find the program of great interest. The material in this course can be helpful to professionals in a variety of functions, such as:
Quality Assurance
Laboratory
Quality Contro
Production
Regulatory Compliance
Engineering
Packaging
Purchasing
Documentation control
Vendors/suppliers
...''
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: New Brunswick
Houses & Roommates: New Brunswick
Other training courses offered by The Center for Professional Advancement:
Sulfonation and Sulfation
Pharmaceutical Process Development
Skin Product Development
Laboratory Control Systems
Pharmaceutical cGMPs and FDA Inspections
Cosmetic Product Formulation
Regulatory Compliance for the Personal Care Products Industry
Clinical Protocols
Hair Product Development
Preparing for and Surviving an FDA Inspection
Patent Law
INDs, NDAs vs CTDs Global Regulations
Granulation, Tabletting and Capsule Technology
System Validation, GAMP Harmonization and P.A.T
Lyophilization Technology
Pharmaceutical Quality Assurance and Control
Critical Process Cleaning and Cleaning Validation
cGMP for Pharmaceutical Production Supervisors
Good Laboratory Practices (GLP)
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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