Training Course:Good Laboratory Practices (GLP)School/Trainer:The Center for Professional Advancement
Millbrae, CA, United States
Course Format: Classroom | E-learning | Virtual Class | Online | On-site | Blended | Self-paced
Course Description:
'' The main intent of this course is to review the requirements imposed by Good Laboratory Practice (GLP) regulations for facilities engaged in, toxicology and product safety testing, primarily in animals and biological test systems. The responsibilities and functions of management, the Study Director, Principal Investigator and the Quality Assurance Unit (QAU) will be covered. Various procedures for meeting the requirements of the regulations will be presented.
The lectures will be supplemented by a question and answer session conducted by the Faculty and by workshops involving problem-solving exercises.
The course will concentrate on OECD Good Laboratory Practice guidelines and their application in member countries, particularly Europe. This will include recent developments regarding multi-site studies and their practical interpretation. Additionally there will be sessions relating to computer validation, particularly as required by FDA in their 21 CFR Part 11 documents.
Emphasis will be placed on practical implementation of GLP and discussion including consideration of problems that the participants bring to the course. Practical hints and recommendations for steps in the implementation of GLP will be included.
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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: Millbrae
Houses & Roommates: Millbrae
Other training courses offered by The Center for Professional Advancement:
Preparing for and Surviving an FDA Inspection
cGMP Auditing - Strategies for Compliance
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
Emulsion-Suspension
Aerosol Technology
Process Analytical Technology
Color Additives and Their Use in Decorative Cosmetics
Industrial Drying of Heat Sensitive Materials
Powder Mixing Technology
GMP for Dietary Supplements
Starch: Chemistry, Properties and Applications
Atomization, Sprays and Atomizers
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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