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Results (61)

Course Title	Course Date	Location
Medical Device Process Validation Training for Professionals	Nov 03, 2025 - Nov 06, 2025
FDA Inspections - What Regulators Expect and How to Prepare	Nov 03, 2025 - Nov 04, 2025
CRO, CDMO and Non-Clinical Vendor Management Fundamentals	Nov 12, 2025 - Nov 14, 2025
Computer System Validation	Nov 12, 2025 - Nov 14, 2025
Biostatistics for Non-Statisticians	Nov 17, 2025 - Nov 20, 2025
Cleaning Validation Best Practices for Drugs, Biologics and Personal Care Products	Nov 18, 2025 - Nov 19, 2025
Writing Effective SOP and Other Process Documents	Nov 18, 2025 - Nov 20, 2025
Integrating Risk Management into the Pharmaceutical Quality System	Dec 01, 2025 - Dec 02, 2025
Auditing and Qualifying Suppliers and Vendors	Dec 02, 2025 - Dec 04, 2025
Good Manufacturing Practices (cGMP) Training	Dec 02, 2025 - Dec 05, 2025
Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirements	Dec 08, 2025 - Dec 11, 2025
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems	Dec 09, 2025 - Dec 11, 2025
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
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
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
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
Computer System Validation	Jul 21, 2026 - Jul 23, 2026
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems	Aug 04, 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
Biostatistics for Non-Statisticians	Nov 02, 2026 - Nov 05, 2026
Medical Device Process Validation Training for Professionals	Nov 02, 2026 - Nov 05, 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
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

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Your privacy and trust are important to us. We collect your information only for operational and advisory purposes. We do not and will not sell your private information to a 3rd party. By agreeing to this policy, you are giving us permission to contact you about our services and courses.