"We provide knowledge and information about CGMP and Quality Systems to the Life Science industry"

Compliance Seminars® - International courses

Our international course program for GMP, Quality Systems, GDP and and Regulatory Affairs professionals in the Pharmaceutical and Medical Device industry. Leading specialist with long experience of training are guiding you through regulations, guidelines, interpretations, requirements and applications.

In addition to the training listed below we offer inhouse training customized for your need. Read more here »

Course program by topic, Pharmaceutical production

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Auditing & Inspections

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GMP Compliance Auditing  #5201

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GMP Compliance and Auditing for Sterile Pharmaceuticals  #5303

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Auditor/Lead Auditor - Preparatory training for certification  #5601

Cleanrooms, Contamination control, Cleaning & Cleaning validation

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Cleaning validation of pharmaceutical process equipment  #5220

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Contamination control in cleanrooms for Life Science production  #5223

Combination products

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US Combination products requirements for the Pharmaceutical & Biotech Industry  #5239

Computers, software, electronic records and signatures

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GMP requirements for Computer Systems & Data Integrity  #5231

GDP (Good Distribution Practice)

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Good Distribution Practice - A Practical Approach  #5222

General GMP Compliance

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Batch Record Review and Investigations  #5301

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Better investigations, better corrective actions  #5243

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CGMP: Interpretation and Application  #5302

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GMP Fast Track  #5311

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GMP/QS Updates - Important news in QA/QM, GMP and Quality Systems  #5126

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From Training to Learning - Improving GMP Performance  #5232

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Procedures for performance: Ways to achieve improved performance  #5242

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Strategic communication - Develop your QA role  #5248

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Writing Incident and Deviation Investigation Reports  #5110

Laboratory Operation

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GMP Compliance for Quality Control and Laboratory Operations  #5202

Risk Management

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Introduction to Risk Assessment and Risk Management for the Pharma and BioPharma Industry   #5111

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Quality Risk Management: Applying the principles and tools  #5221

Statistics

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Valid Statistical Techniques for Medical Device and Pharmaceutical Firms  #5315

Sterile Pharmaceuticals

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GMP Compliance and Auditing for Sterile Pharmaceuticals  #5303

Validation

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Cleaning Validation - Strategy, techniques and regulations  #5220

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Validation and Qualification Compliance Requirements  #5206

Complete training programs

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Auditor/Lead Auditor Pharmaceuticals

Course program by topic, Medical Device production

Hover over the course title for a short description.
Click the title to open the full course description.