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Results (63)




Course Title Course Date Location
Technical Writing for Pharma, Biotech and Med Devices Dec 15, 2025 - Dec 18, 2025
Introduction to Medical Combination Products Jan 12, 2026 - Jan 15, 2026
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management Jan 20, 2026 - Jan 23, 2026
Introduction to Statistical Analysis of Laboratory Data Jan 20, 2026 - Jan 22, 2026
Marketing & Advertising of Pharmaceutical & Medical Devices Jan 26, 2026 - Jan 28, 2026
Writing Effective SOP and Other Process Documents Feb 10, 2026 - Feb 12, 2026
Advanced Topics in Biostatistics for Non-Statisticians Feb 17, 2026 - Feb 19, 2026
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Feb 17, 2026 - Feb 19, 2026
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Feb 23, 2026 - Feb 26, 2026
Good Manufacturing Practices (cGMP) Training Mar 02, 2026 - Mar 05, 2026
Laboratory Equipment Validation and Qualification Mar 02, 2026 - Mar 03, 2026
Medical Device Process Validation Training for Professionals Mar 02, 2026 - Mar 05, 2026
FDA Inspections - What Regulators Expect and How to Prepare Mar 04, 2026 - Mar 05, 2026
Technical Writing for Pharma, Biotech and Med Devices Mar 09, 2026 - Mar 12, 2026
Computer System Validation Mar 10, 2026 - Mar 12, 2026
Biostatistics for Non-Statisticians Mar 16, 2026 - Mar 19, 2026
QbD - Product & Process Optimization using Design of Experiments Mar 16, 2026 - Mar 19, 2026
Cleaning Validation Best Practices for Drugs, Biologics and Personal Care Products Mar 24, 2026 - Mar 25, 2026
Integrating Risk Management into the Pharmaceutical Quality System Apr 07, 2026 - Apr 08, 2026
Auditing and Qualifying Suppliers and Vendors Apr 21, 2026 - Apr 23, 2026
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Apr 21, 2026 - Apr 23, 2026
Introduction to Statistical Analysis of Laboratory Data Apr 28, 2026 - Apr 30, 2026
Writing Effective SOP and Other Process Documents May 12, 2026 - May 14, 2026
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management May 18, 2026 - May 21, 2026
Introduction to Medical Combination Products May 18, 2026 - May 21, 2026
Good Manufacturing Practices (cGMP) Training Jun 01, 2026 - Jun 04, 2026
Technical Writing for Pharma, Biotech and Med Devices Jun 08, 2026 - Jun 11, 2026
Advanced Topics in Biostatistics for Non-Statisticians Jun 09, 2026 - Jun 11, 2026
Marketing & Advertising of Pharmaceutical & Medical Devices Jun 15, 2026 - Jun 17, 2026
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Jun 16, 2026 - Jun 18, 2026
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Jun 22, 2026 - Jun 25, 2026
Biostatistics for Non-Statisticians Jul 06, 2026 - Jul 09, 2026
Laboratory Equipment Validation and Qualification Jul 06, 2026 - Jul 07, 2026
Medical Device Process Validation Training for Professionals Jul 06, 2026 - Jul 09, 2026
FDA Inspections - What Regulators Expect and How to Prepare Jul 08, 2026 - Jul 09, 2026
QbD - Product & Process Optimization using Design of Experiments Jul 13, 2026 - Jul 16, 2026
Computer System Validation Jul 21, 2026 - Jul 23, 2026
Cleaning Validation Best Practices for Drugs, Biologics and Personal Care Products Jul 22, 2026 - Jul 23, 2026
Auditing and Qualifying Suppliers and Vendors Jul 28, 2026 - Jul 30, 2026
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Aug 04, 2026 - Aug 06, 2026
Integrating Risk Management into the Pharmaceutical Quality System Aug 05, 2026 - Aug 06, 2026
Writing Effective SOP and Other Process Documents Aug 11, 2026 - Aug 13, 2026
Good Manufacturing Practices (cGMP) Training Sep 01, 2026 - Sep 04, 2026
Introduction to Statistical Analysis of Laboratory Data Sep 01, 2026 - Sep 03, 2026
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management Sep 14, 2026 - Sep 17, 2026
Technical Writing for Pharma, Biotech and Med Devices Sep 21, 2026 - Sep 24, 2026
Introduction to Medical Combination Products Sep 28, 2026 - Oct 01, 2026
Advanced Topics in Biostatistics for Non-Statisticians Oct 06, 2026 - Oct 08, 2026
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Oct 13, 2026 - Oct 15, 2026
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Oct 19, 2026 - Oct 22, 2026
Marketing & Advertising of Pharmaceutical & Medical Devices Oct 19, 2026 - Oct 21, 2026
QbD - Product & Process Optimization using Design of Experiments Oct 26, 2026 - Oct 29, 2026
Biostatistics for Non-Statisticians Nov 02, 2026 - Nov 05, 2026
Medical Device Process Validation Training for Professionals Nov 02, 2026 - Nov 05, 2026
Cleaning Validation Best Practices for Drugs, Biologics and Personal Care Products Nov 09, 2026 - Nov 10, 2026
FDA Inspections - What Regulators Expect and How to Prepare Nov 09, 2026 - Nov 10, 2026
Laboratory Equipment Validation and Qualification Nov 12, 2026 - Nov 13, 2026
Computer System Validation Nov 17, 2026 - Nov 19, 2026
Writing Effective SOP and Other Process Documents Nov 17, 2026 - Nov 19, 2026
Good Manufacturing Practices (cGMP) Training Dec 01, 2026 - Dec 04, 2026
Auditing and Qualifying Suppliers and Vendors Dec 02, 2026 - Dec 04, 2026
Technical Writing for Pharma, Biotech and Med Devices Dec 07, 2026 - Dec 10, 2026
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Dec 08, 2026 - Dec 10, 2026