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Course Title Course Date Location
OTC Drug and Personal Care Product GMP & FDA Regulation Sep 08, 2025 - Sep 11, 2025
Auditing and Qualifying Suppliers and Vendors Sep 09, 2025 - Sep 11, 2025
Development and Validation of Bioanalytical Assays for Biologics: Quantitation (PK) and Immunogenicity Assays 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
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Sep 16, 2025 - Sep 18, 2025
Implementing an FDA Compliant Stability Program Sep 29, 2025 - Oct 01, 2025
Process Validation for Drugs and Biologics Sep 29, 2025 - Oct 01, 2025
Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries Sep 29, 2025 - Oct 01, 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
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products Oct 09, 2025 - Oct 10, 2025
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Oct 14, 2025 - Oct 16, 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
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Oct 20, 2025 - Oct 23, 2025
Specifications for APIs & Pharmaceutical Drug Products Oct 21, 2025 - Oct 23, 2025
GMP Training for the QC Laboratory Oct 23, 2025 - Oct 24, 2025
QbD - Product & Process Optimization using Design of Experiments Oct 27, 2025 - Oct 30, 2025
Lyophilization Technology - Application of Scientific Principles Oct 28, 2025 - Oct 30, 2025
Preparing the CMC Section for NDAs/INDs/CTDs Oct 29, 2025 - Oct 31, 2025
FDA Inspections - What Regulators Expect and How to Prepare Nov 03, 2025 - Nov 04, 2025
The Drug Development Process from Concept to Market Nov 03, 2025 - Nov 06, 2025
Pharmaceutical Production Batch Record Review Nov 05, 2025 - Nov 07, 2025
CRO, CDMO and Non-Clinical Vendor Management Fundamentals Nov 12, 2025 - Nov 14, 2025
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Nov 12, 2025 - Nov 14, 2025
Computer System Validation Nov 12, 2025 - Nov 14, 2025
CMC Regulatory Compliance Strategy for Cell & Gene Therapy Medicines Nov 17, 2025 - Nov 20, 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
CMC Regulatory Compliance Strategy for Recombinant Proteins, Monoclonal Antibodies, & Biosimilars Dec 08, 2025 - Dec 11, 2025
Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirements Dec 08, 2025 - Dec 11, 2025
Development and Validation of Bioanalytical Assays for Biologics: Quantitation (PK) and Immunogenicity Assays Dec 09, 2025 - Dec 11, 2025
Preparation of FDA Submissions and Communicating with the FDA Dec 10, 2025 - Dec 12, 2025
Technical Writing for Pharma, Biotech and Med Devices Dec 15, 2025 - Dec 18, 2025
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Dec 16, 2025 - Dec 18, 2025