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Facility And Equipment Verification
25-26 Feb 2010
Harrington Hall Hotel, London, United Kingdom
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Facility And Equipment Verification
Description
This seminar will assist you in:
Understanding the link
from product requirements to equipment verification (and hence process validation)
Gaining an understanding of a
practical, science and risk based approach to process equipment verification
Learning about approaches to
laboratory equipment verification
Good Engineering Practice
Unscrambling
the real meaning of the old and new buzz words such as qualification, verification, GEP, commissioning, validation etc.
Find out about
regulatory, quality and engineering requirements
Realising the very significant business benefits
from a science and risk based approach
Practical tools used will include:
ICH Q8-9-10 Guidance
Risk assessment
ASTM E2500 Guide covering verification of pharmaceutical
manufacturing systems and equipment
References to Good Engineering Practice Publications
Use of practical examples
Past Events
Facility And Equipment Verification - 25-26 Feb 2010, Harrington Hall Hotel, London, United Kingdom
(1562)
Important
Please, check "Facility And Equipment Verification" official website for possible changes, before making any traveling arrangements
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Health & Medicine:
Medical device
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