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Results (20)




Course Title Course Date Location
Auditing and Qualifying Suppliers and Vendors Sep 09, 2025 - Sep 11, 2025
Technical Writing for Pharma, Biotech and Med Devices Sep 15, 2025 - Sep 18, 2025
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management Sep 15, 2025 - Sep 18, 2025
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Oct 06, 2025 - Oct 07, 2025
Laboratory Equipment Validation and Qualification Oct 07, 2025 - Oct 08, 2025
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Oct 20, 2025 - Oct 23, 2025
Clinical Trial Project Management, Phase 1-4 Best Practices Oct 20, 2025 - Oct 23, 2025
QbD - Product & Process Optimization using Design of Experiments Oct 27, 2025 - Oct 30, 2025
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Oct 28, 2025 - Oct 30, 2025
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
Writing Effective SOP and Other Process Documents Nov 18, 2025 - Nov 20, 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