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Course Title Course Date Location
Cell and Gene Therapy Product Lifecycle - Introduction Course - Gene Editing, CRISPR/Cas, TALEN Technologies Oct 25, 2023 - Oct 27, 2023
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
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
Computer System Validation Nov 12, 2025 - Nov 14, 2025
Oncology Drug Development Course - A Comprehensive Overview Nov 12, 2025 - Nov 14, 2025
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Nov 13, 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
GMP Auditor Training Nov 17, 2025 - Nov 19, 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
Change Control - GMP Requirements and FDA Enforcement Dec 02, 2025 - Dec 04, 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
RNA Biotechnology - An Introductory Course Dec 08, 2025 - Dec 10, 2025
OTC Drug and Personal Care Product Regulations and GMPs Dec 08, 2025 - Dec 11, 2025
Human Error Prevention (HEP) - Risk Factors and Strategies Dec 09, 2025 - Dec 11, 2025
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Dec 09, 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
Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries Dec 15, 2025 - Dec 17, 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
Introduction to Medical Combination Products Jan 12, 2026 - Jan 15, 2026
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy 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
The Drug Development Process from Concept to Market Jan 26, 2026 - Jan 29, 2026
Pharmaceutical Production Batch Record Review Feb 03, 2026 - Feb 05, 2026
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Feb 03, 2026 - Feb 05, 2026
Writing Effective SOP and Other Process Documents Feb 10, 2026 - Feb 12, 2026
GMP Training for the QC Laboratory Feb 12, 2026 - Feb 13, 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
Preparing the CMC Section for NDAs/INDs/CTDs Feb 24, 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
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Mar 03, 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
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Mar 17, 2026 - Mar 19, 2026
Change Control - GMP Requirements and FDA Enforcement Mar 24, 2026 - Mar 26, 2026
CMC Regulatory Compliance Strategy for Cell & Gene Therapy Medicines Mar 30, 2026 - Apr 02, 2026
OTC Drug and Personal Care Product Regulations and GMPs Apr 07, 2026 - Apr 10, 2026
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Apr 13, 2026 - Apr 16, 2026
Human Error Prevention (HEP) - Risk Factors and Strategies Apr 14, 2026 - Apr 16, 2026
Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries Apr 14, 2026 - Apr 16, 2026
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Apr 21, 2026 - Apr 23, 2026
Preparation of FDA Submissions and Communicating with the FDA Apr 21, 2026 - Apr 23, 2026
The Drug Development Process from Concept to Market Apr 27, 2026 - Apr 30, 2026
Development and Validation of Bioanalytical Assays for Biologics: Quantitation (PK) and Immunogenicity Assays Apr 28, 2026 - Apr 30, 2026
Introduction to Statistical Analysis of Laboratory Data Apr 28, 2026 - Apr 30, 2026
CMC Regulatory Compliance Strategy for Recombinant Proteins, Monoclonal Antibodies, & Biosimilars May 05, 2026 - May 08, 2026
Pharmaceutical Production Batch Record Review May 05, 2026 - May 07, 2026
RNA Biotechnology - An Introductory Course May 12, 2026 - May 14, 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
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Jun 02, 2026 - Jun 04, 2026
GMP Training for the QC Laboratory Jun 08, 2026 - Jun 09, 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
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Jun 16, 2026 - Jun 18, 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
Preparing the CMC Section for NDAs/INDs/CTDs Jun 23, 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
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Jul 07, 2026 - Jul 09, 2026
FDA Inspections - What Regulators Expect and How to Prepare Jul 08, 2026 - Jul 09, 2026
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Jul 13, 2026 - Jul 16, 2026
Change Control - GMP Requirements and FDA Enforcement Jul 14, 2026 - Jul 16, 2026
CMC Regulatory Compliance Strategy for Cell & Gene Therapy Medicines Jul 20, 2026 - Jul 23, 2026
Computer System Validation Jul 21, 2026 - Jul 23, 2026
Preparation of FDA Submissions and Communicating with the FDA Jul 21, 2026 - Jul 23, 2026
OTC Drug and Personal Care Product Regulations and GMPs Jul 27, 2026 - Jul 30, 2026
The Drug Development Process from Concept to Market Jul 27, 2026 - Jul 30, 2026
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Aug 04, 2026 - Aug 06, 2026
Pharmaceutical Production Batch Record Review Aug 04, 2026 - Aug 06, 2026
Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries Aug 11, 2026 - Aug 13, 2026
Writing Effective SOP and Other Process Documents Aug 11, 2026 - Aug 13, 2026
CMC Regulatory Compliance Strategy for Recombinant Proteins, Monoclonal Antibodies, & Biosimilars Aug 17, 2026 - Aug 20, 2026
Human Error Prevention (HEP) - Risk Factors and Strategies Aug 18, 2026 - Aug 20, 2026
Development and Validation of Bioanalytical Assays for Biologics: Quantitation (PK) and Immunogenicity Assays Aug 25, 2026 - Aug 27, 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
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Sep 15, 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
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Sep 29, 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
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Oct 19, 2026 - Oct 22, 2026
Preparing the CMC Section for NDAs/INDs/CTDs Oct 20, 2026 - Oct 22, 2026
GMP Training for the QC Laboratory Oct 22, 2026 - Oct 23, 2026
The Drug Development Process from Concept to Market Oct 26, 2026 - Oct 29, 2026
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Oct 27, 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
Pharmaceutical Production Batch Record Review Nov 03, 2026 - Nov 05, 2026
Preparation of FDA Submissions and Communicating with the FDA Nov 03, 2026 - Nov 05, 2026
RNA Biotechnology - An Introductory Course Nov 03, 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
CMC Regulatory Compliance Strategy for Cell & Gene Therapy Medicines Nov 16, 2026 - Nov 19, 2026
Change Control - GMP Requirements and FDA Enforcement Nov 17, 2026 - Nov 19, 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
OTC Drug and Personal Care Product Regulations and GMPs Dec 01, 2026 - Dec 04, 2026
Development and Validation of Bioanalytical Assays for Biologics: Quantitation (PK) and Immunogenicity Assays Dec 07, 2026 - Dec 09, 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
Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries Dec 08, 2026 - Dec 10, 2026
CMC Regulatory Compliance Strategy for Recombinant Proteins, Monoclonal Antibodies, & Biosimilars Dec 14, 2026 - Dec 17, 2026
Human Error Prevention (HEP) - Risk Factors and Strategies Dec 14, 2026 - Dec 16, 2026
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Dec 15, 2026 - Dec 17, 2026