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Pharmaopportunities has the
largest selection of
Auditing and Inspecting Preclinical Research for GLP Compliance
training courses online. Our training courses are provided by
the some of the best
Biotech
companies in the world.
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| Industry |
Biotech |
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| Training Location |
Amsterdam, The Netherlands Europe
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| Training Date and Time |
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| Seating Capacity |
Not Applicable |
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Description |
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Course Schedule - 1-3 December 2008
This course will explore the activities of a Quality Assurance
department when auditing studies for GLP compliance. All
aspects of QA work will be discussed including; the
preparation of planning documents, review of protocols and
SOPs, inspection of facilities and processes, performance of
inspections of in-life phases and the audit of final reports. The
presenters will consider how an effective rationale can be
developed to provide a solid basis for the implementation of
a QA audit & inspection program. Consideration will be given
to the auditing of suppliers and subcontractors and the role
of QA vis-à-vis computer systems. The reference materials
will be the FDA and OECD Good Laboratory Practice
Regulations and the series of monographs of the OECD
relating to the interpretation of the GLP text. Time will also be
given to the setting up of quantitative techniques for the
measurement of Quality, enabling participants to follow the
compliance level within laboratories.
Lectures will be supplemented with many interactive case
studies, problem solving experiences and workshops.
Emphasis will be on the options available for meeting
regulatory requirements. |
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Who Should Attend |
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This advanced course is designed for Quality Assurance
personnel, or managers wishing to know more about how
best to implement and audit GLP in their facilities. As the
course explores issues innovative to the GLP arena, it
provides an opportunity for experienced personnel to update
their competencies. Participants may come from:-
Industry
- Academia
- Government
- Contract Testing Facilities
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Click here to Download Brochure
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Click here to View Registration Form |
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