| Course Title |
Course Date |
Location |
| Writing Effective SOP and Other Process Documents |
Jan 25, 2021 - Jan 26, 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) |
| Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions |
Feb 17, 2021 - Feb 19, 2021 |
Virtual (London, UK Time) |
| 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) |
| Design Validation, Verification, and Risk Analysis for Medical Device Professionals |
Feb 25, 2021 - Feb 26, 2021 |
Virtual (CST) |
| Introduction to Medical Combination Products |
Mar 02, 2021 - Mar 05, 2021 |
Virtual (London, UK Time) |
| 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) |
| 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) |
| Medical Device Process Validation Training for Professionals |
Mar 24, 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) |
| 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) |
| Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions |
May 24, 2021 - May 25, 2021 |
Virtual (CDT) |
| Marketing & Advertising of Pharmaceutical & Medical Devices |
Jun 22, 2021 - Jun 23, 2021 |
Virtual (CDT) |
| Writing Effective SOP and Other Process Documents |
Sep 20, 2021 - Sep 22, 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) |
| Overview of FDA Regulatory Compliance for Medical Devices |
Oct 18, 2021 - Oct 19, 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) |
