Compliance Seminars^® - International courses
Pharmaceutical production

2019

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

28.11

Effective Quality Management for the Pharmaceutical industry  #5127

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

9-10.12

From Training to Learning - Improving GMP Performance  #5232

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