"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 US GMP, EU GMP, Quality Systems and GDP 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, November 2018 |
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27-28.11 |
GMP requirements for Computer Systems & Data Integrity #5231 |
Copenhagen, December 2018 |
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3-4.12 |
GMP Compliance for Quality Control and Laboratory Operations #5202 |
5-7.12 |
GMP Compliance and Auditing for Sterile Pharmaceuticals #5303 |
6-7.12 |
|
11-12.12 |
Tools to improve poor personnel behaviors - within Pharma and Medical Devices #5251 NEW |
12-13.12 |
Cleaning Validation - Strategy, techniques and regulations #5220 |
2019 |
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Copenhagen, January 2019 |
|
22-24.1 |
Auditor/Lead Auditor - Pharmaceuticals and Medical Devices #5316 |
Copenhagen, April 2019 |
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25-26.4 |
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Copenhagen, May 2019 |
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6.5 |
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7-8.5 |
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9-10.5 |
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20-21.5 |
Quality Risk Management: Applying the principles and tools #5221 |
23-24.5 |
|
28.5 |
Ensure access to the Chinese market - Preparing, Participating and Handling a CFDA Inspection #5128 |
Copenhagen, June 2019 |
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10-12.6 |
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Stockholm, June 2019 |
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10-12.6 |
Valid Statistical Techniques for Medical Device and Pharmaceutical Firms #5315 |
