Available Courses

Results (72)




Course Title Course Date Location
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products Jan 21, 2021 - Jan 22, 2021 Virtual (CST)
Writing Effective SOP and Other Process Documents Jan 25, 2021 - Jan 26, 2021 Virtual (CST)
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Jan 25, 2021 - Jan 27, 2021 Virtual (CST)
Biostatistics for Non-Statisticians Jan 27, 2021 - Jan 29, 2021 Virtual (CST)
Auditing and Qualifying Suppliers and Vendors Jan 28, 2021 - Jan 29, 2021 Virtual (CST)
Process Validation for Drugs and Biologics Feb 01, 2021 - Feb 02, 2021 Virtual (CST)
Developability Assessment – The Logical Approach to Discovery Lead Selection Feb 04, 2021 - Feb 05, 2021 Virtual (CST)
Basic GMP Training for the QC Laboratory Feb 04, 2021 - Feb 05, 2021 Virtual (CST)
Stability Programs for Determining Product Shelf Life Feb 08, 2021 - Feb 09, 2021 Virtual (CST)
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Feb 10, 2021 - Feb 12, 2021 Virtual (CST)
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Feb 17, 2021 - Feb 19, 2021 Virtual (London, UK Time)
Pharmaceutical Production Batch Record Review | Training Feb 18, 2021 - Feb 19, 2021 Virtual (CST)
Technical Writing for Pharma, Biotech and Med Devices Feb 22, 2021 - Feb 24, 2021 Virtual (CST)
Design Control for Medical Device Professionals Feb 22, 2021 - Feb 23, 2021 Virtual (CST)
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Feb 24, 2021 - Feb 26, 2021 Virtual (CST)
Best Practices for an Effective Cleaning Validation Program Feb 25, 2021 - Feb 26, 2021 Virtual (CST)
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Feb 25, 2021 - Feb 26, 2021 Virtual (CST)
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Mar 01, 2021 - Mar 02, 2021 Virtual (CST)
Introduction to Medical Combination Products Mar 02, 2021 - Mar 05, 2021 Virtual (London, UK Time)
Development and Validation of Bioanalytical Assays for Biologics Quantitation and Immunogenicity Assays Mar 04, 2021 - Mar 05, 2021 Virtual (CST)
FDA Inspections - What Regulators Expect and How to Prepare Mar 04, 2021 - Mar 05, 2021 Virtual (CST)
Laboratory Equipment Validation and Qualification Mar 08, 2021 - Mar 09, 2021 Virtual (CST)
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Mar 08, 2021 - Mar 09, 2021 Virtual (CST)
Computer System Validation Mar 08, 2021 - Mar 09, 2021 Virtual (CST)
The Drug Development Process from Concept to Market Mar 08, 2021 - Mar 10, 2021 Virtual (CST)
Molecular Biology Techniques – Applications in the Biotechnology and Pharmaceutical Industries Mar 10, 2021 - Mar 12, 2021 Virtual (CST)
Preparing the CMC Section for NDAs/INDs/CTDs Mar 11, 2021 - Mar 12, 2021 Virtual (CST)
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management Mar 15, 2021 - Mar 16, 2021 Virtual (CDT)
Understanding & Implementing New EU Clinical Trial Regulation & GDPR Mar 15, 2021 - Mar 16, 2021 Virtual (CDT)
Effective Document Management for Pharma, Biotech & Medical Device Mar 18, 2021 - Mar 19, 2021 Virtual (CDT)
GMPs for OTC & Cosmetic Products - US and Global Requirements Mar 18, 2021 - Mar 19, 2021 Virtual (CDT)
Preparation of FDA Submissions and Communicating with the FDA Mar 22, 2021 - Mar 23, 2021 Virtual (CDT)
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Mar 22, 2021 - Mar 23, 2021 Virtual (CDT)
Medical Device Process Validation Training for Professionals Mar 24, 2021 - Mar 26, 2021 Virtual (CDT)
Lyophilization Technology-Application of Scientific Principles Mar 25, 2021 - Mar 26, 2021 Virtual (CDT)
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Apr 08, 2021 - Apr 09, 2021 Virtual (CDT)
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Apr 12, 2021 - Apr 13, 2021 Virtual (CDT)
European Regulatory Procedures - EMA & National Requirements Apr 15, 2021 - Apr 16, 2021 Virtual (London, UK Time)
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Apr 19, 2021 - Apr 21, 2021 Virtual (London, UK Time)
Good Manufacturing Practices Training | GMP Course Apr 20, 2021 - Apr 23, 2021 Virtual (London, UK Time)
Selecting and Managing CROs Apr 22, 2021 - Apr 23, 2021 Virtual (CDT)
Integration of Risk Management Principles and Activities into the Quality System Apr 22, 2021 - Apr 23, 2021 Virtual (CDT)
Overview of FDA Regulatory Compliance for Medical Devices Apr 26, 2021 - Apr 27, 2021 Virtual (CDT)
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials May 06, 2021 - May 07, 2021 Virtual (London, UK Time)
Introduction to Medical Combination Products May 10, 2021 - May 12, 2021 Virtual (CDT)
Computer System Validation May 11, 2021 - May 13, 2021 Virtual (London, UK Time)
US Cosmetic Regulation: FDA CFR Title 21 Training May 12, 2021 - May 14, 2021 Virtual (CDT)
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals May 17, 2021 - May 19, 2021 Virtual (CDT)
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products May 19, 2021 - May 21, 2021 Virtual (London, UK Time)
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions May 24, 2021 - May 25, 2021 Virtual (CDT)
European Regulatory Procedures - EMA & National Requirements Jun 10, 2021 - Jun 11, 2021 Virtual (EDT)
Marketing & Advertising of Pharmaceutical & Medical Devices Jun 22, 2021 - Jun 23, 2021 Virtual (CDT)
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Jun 22, 2021 - Jun 24, 2021 Virtual (London, UK Time)
Preparation of FDA Submissions and Communicating with the FDA Jun 23, 2021 - Jun 25, 2021 Virtual (London, UK Time)
Good Manufacturing Practices Training | GMP Course Jul 21, 2021 - Jul 23, 2021 Virtual (CDT)
Writing Effective SOP and Other Process Documents Sep 20, 2021 - Sep 22, 2021 Virtual (London, UK Time)
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management Sep 20, 2021 - Sep 21, 2021 Virtual (London, UK Time)
Basic GMP Training for the QC Laboratory Sep 27, 2021 - Sep 29, 2021 Virtual (London, UK Time)
Biostatistics for Non-Statisticians Oct 04, 2021 - Oct 07, 2021 Virtual (London, UK Time)
Auditing and Qualifying Suppliers and Vendors Oct 06, 2021 - Oct 08, 2021 Virtual (London, UK Time)
The Drug Development Process from Concept to Market Oct 12, 2021 - Oct 15, 2021 Virtual (London, UK Time)
Overview of FDA Regulatory Compliance for Medical Devices Oct 18, 2021 - Oct 19, 2021 Virtual (London, UK Time)
Best Practices for an Effective Cleaning Validation Program Oct 18, 2021 - Oct 20, 2021 Virtual (London, UK Time)
Developability Assessment – The Logical Approach to Discovery Lead Selection Oct 28, 2021 - Oct 29, 2021 Virtual (London, UK Time)
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products Nov 04, 2021 - Nov 05, 2021 Virtual (London, UK Time)
Technical Writing for Pharma, Biotech and Med Devices Nov 08, 2021 - Nov 11, 2021 Virtual (London, UK Time)
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Nov 08, 2021 - Nov 11, 2021 Virtual (London, UK Time)
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Nov 15, 2021 - Nov 18, 2021 Virtual (London, UK Time)
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Nov 17, 2021 - Nov 19, 2021 Virtual (London, UK Time)
Development and Validation of Bioanalytical Assays for Biologics Quantitation and Immunogenicity Assays Dec 01, 2021 - Dec 03, 2021 Virtual (London, UK Time)
Stability Programs for Determining Product Shelf Life Dec 08, 2021 - Dec 10, 2021 Virtual (London, UK Time)
Clinical Trial Project Management, Phase 1-4 Best Practices Dec 15, 2021 - Dec 16, 2021 Virtual (EST)