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

Compliance Seminars® - International courses
Pharmaceutical production

Our international course program for GMP, QS, GDP and GEP professionals in the pharmaceutical industry. Leading specialist with long experience of training are guiding you through regulations, guidelines, interpretations, requirements and applications.

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
Co-organized with Symbioteq

Biopharmaceuticals & Biotechnology

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FDA Expectations for Biopharmaceutical/Biologic API Process Validation  #5213

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GMP Compliance and Auditing for Biopharmaceutical/Biologic APIs  #5310

CAPA

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Investigations & CAPA - Training on the entire CA/PA Lifecycles  #5238

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

Clinical Trial Materials

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Best Practices for Global Investigational Medicinal Product (IMP) Management  #5219

Combination products

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

GDP (Good Distribution Practice)

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Good Distribution Practice, compliance essentials and effective implementation techniques  #5119

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Good Distribution Practice - A Practical Approach  #5222

GEP (Good Engineering Practice)

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Good Engineering Practice (GEP) - A Practical Approach for Engineers  #5224

General GMP Compliance

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Batch Record Review and Investigations  #5301

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Better Ways to Investigate and Document Incidents  #5234

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Better investigations, better corrective actions  #5243

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Beyond GMP - Most companies achieve good levels of GMP compliance, so where next?  #5235

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CGMP: Interpretation and Application  #5302

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Change Control training  #5240

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GMP Compliance for Biopharmaceutical/Biologic APIs  #5310

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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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Leading the climb for Compliance: GMPs for supervisors & quality unit members  #5229

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Procedures for performance: Ways to achieve improved performance  #5242

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Procedures for performance  #5109

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Qualified Person Update - working with the modernised Annex 16 and supply chain overview  #5114

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Quality Change Management Workshop  #5236

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Technical Writing and Documenting Investigations  #5241

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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

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    Major update!

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FDA Expectations for Biopharmaceutical/Biologic API Process Validation  #5213

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Technical Writing: Writing Validation Documents  #5237

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Validation and Qualification Compliance Requirements  #5206