| Course Title |
Course Date |
Location |
| Effective Document Management for Pharma, Biotech & Medical Device |
Jan 27, 2020 - Jan 28, 2020 |
Los Angeles, CA United States of America |
| Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy |
Feb 05, 2020 - Feb 07, 2020 |
Malvern, PA United States of America |
| Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies |
Feb 24, 2020 - Feb 26, 2020 |
Malvern, PA United States of America |
| Auditing and Qualifying Suppliers and Vendors |
Feb 27, 2020 - Feb 28, 2020 |
Malvern, PA United States of America |
| Design Control for Medical Device Professionals |
Mar 02, 2020 - Mar 03, 2020 |
Malvern, PA United States of America |
| Design Validation, Verification, and Risk Analysis for Medical Device Professionals |
Mar 04, 2020 - Mar 05, 2020 |
Malvern, PA United States of America |
| Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems |
Mar 05, 2020 - Mar 06, 2020 |
Malvern, PA United States of America |
| Understanding & Implementing New EU Clinical Trial Regulation & GDPR |
Mar 05, 2020 - Mar 06, 2020 |
Malvern, PA United States of America |
| Integration of Risk Management Principles and Activities into the Quality System |
Mar 09, 2020 - Mar 10, 2020 |
Malvern, PA United States of America |
| Writing Effective SOP and Other Process Documents |
Mar 09, 2020 - Mar 10, 2020 |
Dublin, Ireland |
| Medical Device Process Validation Training for Professionals |
Mar 11, 2020 - Mar 13, 2020 |
Malvern, PA United States of America |
| Technical Writing for Pharma, Biotech and Med Devices |
Mar 11, 2020 - Mar 13, 2020 |
Dublin, Ireland |
| Overview of FDA Regulatory Compliance for Medical Devices |
Mar 16, 2020 - Mar 17, 2020 |
Malvern, PA United States of America |
| Qualifying, Management and Auditing of Contract Manufacturing Organizations |
Mar 16, 2020 - Mar 17, 2020 |
Malvern, PA United States of America |
| FDA Inspections - What Regulators Expect and How to Prepare |
Mar 19, 2020 - Mar 20, 2020 |
Malvern, PA United States of America |
| GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials |
Mar 19, 2020 - Mar 20, 2020 |
Malvern, PA United States of America |
| Writing Effective SOP and Other Process Documents |
Mar 23, 2020 - Mar 24, 2020 |
Malvern, PA United States of America |
| Technical Writing for Pharma, Biotech and Med Devices |
Mar 25, 2020 - Mar 27, 2020 |
Malvern, PA United States of America |
| Computer System Validation |
Mar 30, 2020 - Mar 31, 2020 |
Malvern, PA United States of America |
| Marketing & Advertising of Pharmaceutical & Medical Devices |
Mar 30, 2020 - Mar 31, 2020 |
Boston, MA United States of America |
| Biostatistics for Non-Statisticians |
Apr 01, 2020 - Apr 03, 2020 |
Boston, MA United States of America |
| Clinical Trial Design For Medical Devices™ |
Apr 06, 2020 - Apr 07, 2020 |
Los Angeles, CA United States of America |
| Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries |
Apr 06, 2020 - Apr 07, 2020 |
Los Angeles, CA United States of America |
| Selecting and Managing CROs |
Apr 23, 2020 - Apr 24, 2020 |
Los Angeles, CA United States of America |
| Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy |
Apr 29, 2020 - May 01, 2020 |
London, United Kingdom |
| Effective Document Management for Pharma, Biotech & Medical Device |
May 04, 2020 - May 05, 2020 |
Boston, MA United States of America |
| Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions |
May 04, 2020 - May 05, 2020 |
Los Angeles, CA United States of America |
| Introduction to Medical Combination Products |
May 06, 2020 - May 08, 2020 |
Los Angeles, CA United States of America |
| QbD - Product & Process Optimization using Design of Experiments |
May 11, 2020 - May 13, 2020 |
London, United Kingdom |
| Design Control for Medical Device Professionals |
Jun 08, 2020 - Jun 09, 2020 |
Chicago, IL United States of America |
| Design Validation, Verification, and Risk Analysis for Medical Device Professionals |
Jun 10, 2020 - Jun 11, 2020 |
Chicago, IL United States of America |
| Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy |
Jun 10, 2020 - Jun 12, 2020 |
Boston, MA United States of America |
| Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies |
Jun 15, 2020 - Jun 17, 2020 |
Chicago, IL United States of America |
| Auditing and Qualifying Suppliers and Vendors |
Jun 25, 2020 - Jun 26, 2020 |
Boston, MA United States of America |
| FDA Inspections - What Regulators Expect and How to Prepare |
Jul 20, 2020 - Jul 21, 2020 |
Boston, MA United States of America |
| Qualifying, Management and Auditing of Contract Manufacturing Organizations |
Jul 27, 2020 - Jul 28, 2020 |
Boston, MA United States of America |
| Auditing and Qualifying Suppliers and Vendors |
Sep 24, 2020 - Sep 25, 2020 |
London, United Kingdom |
| Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems |
Oct 05, 2020 - Oct 06, 2020 |
London, United Kingdom |
| Medical Device Process Validation Training for Professionals |
Oct 07, 2020 - Oct 09, 2020 |
London, United Kingdom |
| Design Control for Medical Device Professionals |
Oct 12, 2020 - Oct 13, 2020 |
London, United Kingdom |
| Design Validation, Verification, and Risk Analysis for Medical Device Professionals |
Oct 14, 2020 - Oct 15, 2020 |
London, United Kingdom |
