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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

Online webinar, August 2020

24.8

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

September 2020

15-16.9

Strategic communication - Develop your QA role  #5248  Copenhagen

14-17.9

GMP FastTrack  #5311    ON-LINE

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

19-20.10

Tools to Decrease Human Errors within Life Science Organisations  #5251

20-22.10

Valid Statistical Techniques Made Easy  #5315

21-22.10

Aseptic Manufacturing – Maintaining the validated state  #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

8.12

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

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

8-9.12

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, 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

On-Line, September 2020

15.9

Risk Management according to 14971:2019  #5135    ON-LINE

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

19-20.10

Tools to Decrease Human Errors within Life Science Organisations  #5251

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

9-10/12

Clinical Evaluation for Medical Devices - based on MEDDEV 2.7/1 rev 4 and the MDR  #5256

11.12

Medical Device Postmarket Surveillance - PMS   #5123

Registration