"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, June 2018 |
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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 NEW |
Copenhagen, November 2018 |
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6-7.11 |
Cleaning Validation - Strategy, techniques and regulations #5220 |
6-8.11 |
|
27-28.11 |
GMP requirements for Computer Systems & Data Integrity #5231 |
27-29.11 |
Valid Statistical Techniques for Medical Device and Pharmaceutical Firms #5315 |
Copenhagen, December 2018 |
|
3-4.12 |
GMP Compliance for Quality Control and Laboratory Operations #5202 |
3-4.12 |
Procedures for performance: Ways to achieve improved performance #5242 |
5-7.12 |
GMP Compliance and Auditing for Sterile Pharmaceuticals #5303 |
6-7.12 |
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11-12.12 |
Tools to improve poor personnel behaviors - within Pharma and Medical Devices #5251 NEW |
2019 |
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Copenhagen, January 2019 |
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22-24.1 |
Auditor/Lead Auditor - Pharmaceuticals and Medical Devices #5316 |
