"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, QS, GDP and GEP 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.

Course program by topic, Pharmaceutical production

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

»

GMP Compliance Auditing  #5201

»

GMP Compliance and Auditing for Sterile Pharmaceuticals  #5303

»

Auditor/Lead Auditor - Preparatory training for certification  #5601

Cleanrooms, Contamination control, Cleaning & Cleaning validation

»

Cleaning validation of pharmaceutical process equipment  #5220

»

Contamination control in cleanrooms for Life Science production  #5223

Combination products

»

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

Computers, software, electronic records and signatures

»

GMP requirements for Computer Systems & Data Integrity  #5231

GDP (Good Distribution Practice)

»

Good Distribution Practice - A Practical Approach  #5222

General GMP Compliance

»

Batch Record Review and Investigations  #5301

»

Better investigations, better corrective actions  #5243

»

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

»

CGMP: Interpretation and Application  #5302

»

GMP Fast Track  #5311

»

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

»

From Training to Learning - Improving GMP Performance  #5232

»

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

»

Procedures for performance: Ways to achieve improved performance  #5242

»

Procedures for performance  #5109

»

Strategic communication - Develop your QA role  #5248

»

Writing Incident and Deviation Investigation Reports  #5110

Laboratory Operation

»

GMP Compliance for Quality Control and Laboratory Operations  #5202

Risk Management

»

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

»

Quality Risk Management: Applying the principles and tools  #5221

Statistics

»

Valid Statistical Techniques for Medical Device and Pharmaceutical Firms  #5315

Sterile Pharmaceuticals

»

GMP Compliance and Auditing for Sterile Pharmaceuticals  #5303

Validation

»

Cleaning Validation - Strategy, techniques and regulations  #5220

»

Validation and Qualification Compliance Requirements  #5206

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.
Auditing & Inspections

»

Auditor/Lead Auditor - Preparatory training for certification  #5601

CAPA

»

Corrective and Preventive Action (CAPA) Requirements and Industry Practice  #5308

Cleanrooms, Contamination control, Cleaning & Cleaning validation

»

Contamination control in cleanrooms for Life Science production  #5223

Computers, software, electronic records and signatures

»

Validation of software for QMS process  #5121

Design Control

»

Design Controls - in a Nutshell   #5115

»

Design Control Requirements and Industry Practice  #5307

General GMP / QS Compliance

»

Better investigations, better corrective actions  #5243

»

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

»

From Training to Learning - Improving GMP Performance  #5232

»

Management Responsibility - in a Nutshell   #5118

»

Medical device quality management - Key requirements in MDR, QSReg and ISO13485  #5314

»

Procedures for performance: Ways to achieve improved performance  #5242

»

QA/RA Leader Medical Devices - Preparatory training for certification  #5502

»

Quality System for Medical Devices in compliance with ISO 13485 #5245

»

Quality System Requirements & Industry Practice  #5501

»

Quality System Regulation - in a Nutshell   #5116

»

Risk-Based Decision Making - in a Nutshell   #5117

»

Strategic communication - Develop your QA role  #5248

»

The new European regulatory landscape – MDR and IVDR - Conference  #5120

Statistics

»

Valid Statistical Techniques for Medical Device and Pharmaceutical Firms  #5315

Validation

»

Process Validation Requirements and Industry Practice  #5309

»

Technical Writing: Writing Validation Documents  #5237