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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.

2020

Copenhagen, May 2020

26.5

Biocleaning: Cleaning and decontamination of surfaces in cleanrooms and apparatus  #5125  Postponed to 11 June 2020 due to covid-19

27-28.5

Cleaning Validation - Strategy, techniques and regulations  #5220  Postponed to 16-17 December 2020 (Amsterdam) due to covid-19

Online webinar, June 2020

3.6

Corrective Action Planning – Keys to Success   #5815    WEBINAR

22.6

Equipment Management in the Pharmaceutical Supply Chain; with a Focus on Calibration   #5820    WEBINAR

Copenhagen, June 2020

2-4.6

Valid Statistical Techniques Made Easy  #5315  Postponed October/November 2020 due to covid-19

9-10.6

Understanding the new draft of Annex 1 - Manufacture of Sterile Medicinal Products  #5230  Postponed to 3-4 December 2020 (Amsterdam) due to covid-19

11.6

Biocleaning: Cleaning and decontamination of surfaces in cleanrooms and apparatus  #5125  Postponed to 15 December 2020 (Amsterdam) due to covid-19

11-12.6

Strategic communication - Develop your QA role  #5248  Postponed to 15-16 September 2020 due to covid-19

15.6

GMP responsibilities for MAH – new draft from EMA  #5809    WEBINAR

15-16.6

GMP Compliance Auditing  #5201  Postponed to 1-2 December 2020 due to covid-19

16.6

Decontamination Process and the new Draft of the EU GMP Annex 1  #5818    WEBINAR

17-18.6

Validation and Qualification Compliance Requirements  #5206  Postponed to 3-4 December 2020 due to covid-19

18.6

New perspectives on Cross Contamination and Cleaning validation  #5819    WEBINAR

Copenhagen, September 2020

15-16.9

Strategic communication - Develop your QA role  #5248

15-17.9

GMP FastTrack  #5311

Copenhagen, October 2020

5-6.10

From Training to Learning - Improving GMP Performance  #5232

8-9.10

Effective root cause investigation for Life Science  #5243

21-22.10

Aseptic Manufacturing – Maintaining the validated state, Conference  #5255  CONFERENCE

Amsterdam, October 2020

6-7.10

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

6-7.10

The application of Good Distribution Practice (GDP) for the Responsible Person handling Pharmaceuticals  #5257

Copenhagen, November 2020

3-5.11

Auditor/Lead Auditor - Pharmaceuticals and Medical Devices  #5316

Amsterdam, December 2020

2.12

Contamination Control Strategy  #5124

3-4.12

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

16-17.12

Cleaning Validation - Strategy, techniques and regulations  #5220

15.12

Biocleaning: Cleaning and decontamination of surfaces in cleanrooms and apparatus  #5125

Copenhagen, December 2020

1-2.12

GMP Compliance Auditing  #5201

3-4.12

Validation and Qualification Compliance Requirements  #5206

7-8.12

GMP Compliance for Quality Control and Laboratory Operations  #5202

8.12

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

8-9.12

GMP requirements for Computer Systems & Data Integrity  #5231

9-11.12

GMP Compliance and Auditing for Sterile Pharmaceuticals  #5303

 

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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.

2020

Online webinar, June 2020

3.6

Corrective Action Planning – Keys to Success   #5815    WEBINAR

Copenhagen, June 2020

2-3.6

Clinical Evaluation for Medical Devices - based on MEDDEV 2.7/1 rev 4 and the MDR  #5256  Postponed to October/November 2020 due to covid-19

2-4.6

Valid Statistical Techniques Made Easy  #5315  Postponed to 20-22 October 2020 due to covid-19

4.6

Medical Device Postmarket Surveillance - PMS   #5123  ONLINE

11-12.6

Strategic communication - Develop your QA role  #5248  Postponed to 15-16 September 2020 due to covid-19

16-18.6

QA/RA Leader Medical Devices - Unique training to become certified QA-RA Leader  #5317  Postponed 8-10 December 2020 due to covid-19

Online webinar, September 2020

1.9

Acceptance Sampling Plans: Inspection by Attributes   #5821    WEBINAR

Copenhagen, September 2020

15-16.9

Strategic communication - Develop your QA role  #5248

Amsterdam, September 2020

15.9

Risk Management according to 14971:2019  #5135

Online webinar, October 2020

9.10

Acceptance Sampling Plans: Inspection by Variables   #5822    WEBINAR

Copenhagen, October 2020

5-6.10

From Training to Learning - Improving GMP Performance  #5232

7-8.10

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

8-9.10

Effective root cause investigation for Life Science  #5243

9.10

Validation of software for QMS process  #5121

20-22.10

Valid Statistical Techniques Made Easy  #5315

Copenhagen, November 2020

3-5.11

Auditor/Lead Auditor - Pharmaceuticals and Medical Devices  #5316

16-17.11

Effective Design Controls, Outstanding Products  #5249

16-18.11

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

18.11

Essential Corrective Action and Preventive Action Practices  #5129

Copenhagen, December 2020

8.12

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

8-10.12

QA/RA Leader Medical Devices - Unique training to become certified QA-RA Leader  #5317

Registration