"We provide knowledge and information about CGMP and Quality Systems to the Life Science industry"
Compliance Seminars® - International courses
Pharmaceutical production
Our international course program for GMP, QS, GDP and GEP professionals in the pharmaceutical industry. Leading specialist with long experience of training are guiding you through regulations, guidelines, interpretations, requirements and applications.
Hover over the course title for a short description.
Click the title to open the full course description with dates, locations and pricing.
2018 |
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Copenhagen, May 2018 |
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14-15.5 |
Quality Risk Management: Applying the principles and tools #5221 |
16-17.5 |
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29-30.5 |
|
29-30.5 |
Cleaning Validation - Strategy, techniques and regulations #5220 |
Copenhagen, June 2018 |
|
11-12.6 |
|
12-13.6 |
GMP requirements for Computer Systems & Data Integrity #5231 |
12-13.6 |
|
13-14.6 |
|
19.6 |
Effective Quality Management - for Pharma and Medical Devices #5127 |
19-20.6 |
Understanding the new draft of Annex 1 - Manufacture of Sterile Medicinal Products #5230 |
Copenhagen, October 2018 |
|
9.10 |
Ensure access to the Chinese market - Preparing, Participating and Handling a CFDA Inspection #5128 |
Copenhagen, November 2018 |
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6-8.11 |
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27-29.11 |
Valid Statistical Techniques for Medical Device and Pharmaceutical Firms #5315 |
