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Course Calendar, Pharmaceutical production

Hover over the course title for a short description.
Click the title to open the full course description with dates, locations and pricing.

2019

Copenhagen, May 2019

20-21.5

Quality Risk Management: Applying the principles and tools  #5221

23-24.5

From Training to Learning - Improving GMP Performance  #5232

Copenhagen, June 2019

11-13.6

GMP FastTrack  #5311

Stockholm, June 2019

10-12.6

Valid Statistical Techniques Made Easy  #5315

Copenhagen, September 2019

17-19.9

Auditor/Lead Auditor - Pharmaceuticals and Medical Devices  #5316

Copenhagen, October 2019

23-24.10

Science, Risk and Statistics-based Cleaning Process Development and Validation  #5254   CONFERENCE

Copenhagen, November 2019

25-26.11

GMP Compliance for Quality Control and Laboratory Operations  #5202

27-28.11  

Tools to decrease human errors – within Life Science Organisations  #5251

27-29.11

GMP Compliance and Auditing for Sterile Pharmaceuticals  #5303

Copenhagen, December 2019

3-4.12

GMP requirements for Computer Systems & Data Integrity  #5231

3-4.12

Understanding the new draft of Annex 1 - Manufacture of Sterile Medicinal Products  #5230

5.12

Contamination Control Strategy  #5124

5-6.12

Strategic communication - Develop your QA role  #5248

5-6.12   

Better investigations, better corrective actions  #5243

10-11.12

Cleaning Validation - Strategy, techniques and regulations  #5220

12.12

Biocleaning: Cleaning and decontamination of surfaces in classified areas and equipment  #5125

12.12

Ensure access to the Chinese market - Preparing, Participating and Handling a CFDA Inspection   #5128

17.12

GDocP – Good Documentation Practices   #5133

 

Registration    

Course calendar, Medical Device production

Hover over the course title for a short description.
Click the title to open the full course description with dates, locations and pricing.

2019

Copenhagen, May 2019

23-24.5

From Training to Learning - Improving GMP Performance  #5232

Stockholm, June 2019

10-12.6

Valid Statistical Techniques Made Easy  #5315

Copenhagen, June 2019

11-12.6

Requirements to place Medical Device Software and Health Software on the market  #5252  NEW

13.6

Validation of software for QMS process  #5121

On-line webinar, September 2019

9.9

Test Method Validation (TMV) Made Easy - Part 1  #5803    WEBINAR

Copenhagen, September 2019

17-19.9

Auditor/Lead Auditor - Pharmaceuticals and Medical Devices  #5316

24-26.9

Medical Device Quality Management Systems (QMS) - Key requirements in ISO 13485, MDR and QSReg  #5314

Gothenburg, October 2019

1-2.10

The 3rd Symbioteq Biocompatibility Medical Devices Conference 2019  #5247

On-line webinar, October 2019

14.10

Test Method Validation (TMV) Made Easy - Part 2  #5804    WEBINAR

Copenhagen, November 2019

4-5.11

Effective Design Controls, Outstanding Products  #5249

6.11

Essential Corrective Action and Preventive Action Practices  #5129

26-27.11

Creating a successful clinical strategy for your Medical Device - Do’s and Dont’s  #5253

27-28.11  

Tools to decrease human errors – within Life Science Organisations  #5251

Copenhagen, December 2019

5-6.12

Strategic communication - Develop your QA role  #5248

5-6.12   

Better investigations, better corrective actions  #5243

12.12

Ensure access to the Chinese market - Preparing, Participating and Handling a CFDA Inspection   #5128

17.12

GDocP – Good Documentation Practices   #5133

Registration