| Course Title |
Course Date |
Location |
| Marketing & Advertising of Pharmaceutical & Medical Devices |
Jun 02, 2020 - Jun 03, 2020 |
Virtual (EDT), |
| Auditing and Qualifying Suppliers and Vendors |
Jun 25, 2020 - Jun 26, 2020 |
Virtual (EDT), |
| Computer System Validation |
Jul 13, 2020 - Jul 14, 2020 |
Virtual (PDT), |
| Medical Devices: The New MDRs, EU Directives, Guidance, CE Marking and ISO Standard Certifications |
Jul 16, 2020 - Jul 17, 2020 |
Virtual (EDT), |
| FDA Inspections - What Regulators Expect and How to Prepare |
Jul 20, 2020 - Jul 21, 2020 |
Virtual (EDT), |
| Writing Effective SOP and Other Process Documents |
Jul 20, 2020 - Jul 21, 2020 |
Virtual (PDT), |
| Biostatistics for Non-Statisticians |
Jul 21, 2020 - Jul 23, 2020 |
Virtual (EDT), |
| Technical Writing for Pharma, Biotech and Med Devices |
Jul 22, 2020 - Jul 24, 2020 |
Virtual (PDT), |
| Qualifying, Management and Auditing of Contract Manufacturing Organizations |
Jul 27, 2020 - Jul 28, 2020 |
Virtual (EDT), |
| Integration of Risk Management Principles and Activities into the Quality System |
Jul 27, 2020 - Jul 28, 2020 |
Virtual (PDT), |
| Medical Device Process Validation Training for Professionals |
Jul 29, 2020 - Jul 31, 2020 |
Virtual (PDT), |
| Design Control for Medical Device Professionals |
Aug 10, 2020 - Aug 11, 2020 |
Virtual (CDT), |
| Design Validation, Verification, and Risk Analysis for Medical Device Professionals |
Aug 12, 2020 - Aug 13, 2020 |
Virtual (EDT), |
| Technical Writing for Pharma, Biotech and Med Devices |
Sep 09, 2020 - Sep 11, 2020 |
Malvern, PA United States of America |
| Effective Document Management for Pharma, Biotech & Medical Device |
Sep 14, 2020 - Sep 15, 2020 |
Malvern, PA United States of America |
| GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials |
Sep 14, 2020 - Sep 15, 2020 |
Los Angeles, CA United States of America |
| Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems |
Sep 21, 2020 - Sep 22, 2020 |
Boston, MA United States of America |
| Auditing and Qualifying Suppliers and Vendors |
Sep 24, 2020 - Sep 25, 2020 |
London, United Kingdom |
| Overview of FDA Regulatory Compliance for Medical Devices |
Sep 24, 2020 - Sep 25, 2020 |
Los Angeles, CA United States of America |
| Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems |
Oct 05, 2020 - Oct 06, 2020 |
London, United Kingdom |
| Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies |
Oct 05, 2020 - Oct 07, 2020 |
Boston, MA United States of America |
| Medical Device Process Validation Training for Professionals |
Oct 07, 2020 - Oct 09, 2020 |
London, United Kingdom |
| Biostatistics for Non-Statisticians |
Oct 07, 2020 - Oct 09, 2020 |
Malvern, PA United States of America |
| 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 |
| Auditing and Qualifying Suppliers and Vendors |
Oct 15, 2020 - Oct 16, 2020 |
Los Angeles, CA United States of America |
| Selecting and Managing CROs |
Oct 15, 2020 - Oct 16, 2020 |
Boston, MA United States of America |
| Clinical Trial Design For Medical Devices™ |
Oct 19, 2020 - Oct 20, 2020 |
Malvern, PA United States of America |
| Integration of Risk Management Principles and Activities into the Quality System |
Oct 19, 2020 - Oct 20, 2020 |
Boston, MA United States of America |
| Medical Device Process Validation Training for Professionals |
Oct 21, 2020 - Oct 23, 2020 |
Boston, MA United States of America |
| Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy |
Oct 21, 2020 - Oct 23, 2020 |
Los Angeles, CA United States of America |
| Qualifying, Management and Auditing of Contract Manufacturing Organizations |
Oct 22, 2020 - Oct 23, 2020 |
Los Angeles, CA United States of America |
| Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries |
Oct 22, 2020 - Oct 23, 2020 |
Malvern, PA United States of America |
| Medical Devices: The New MDRs, EU Directives, Guidance, CE Marking and ISO Standard Certifications |
Oct 26, 2020 - Oct 27, 2020 |
Boston, MA United States of America |
| Computer System Validation |
Nov 09, 2020 - Nov 10, 2020 |
Boston, MA United States of America |
| Design Control for Medical Device Professionals |
Nov 09, 2020 - Nov 10, 2020 |
Boston, MA United States of America |
| FDA Inspections - What Regulators Expect and How to Prepare |
Nov 09, 2020 - Nov 10, 2020 |
Los Angeles, CA United States of America |
| Technical Writing for Pharma, Biotech and Med Devices |
Nov 11, 2020 - Nov 13, 2020 |
Boston, MA United States of America |
| Design Validation, Verification, and Risk Analysis for Medical Device Professionals |
Nov 11, 2020 - Nov 12, 2020 |
Boston, MA United States of America |
| Marketing & Advertising of Pharmaceutical & Medical Devices |
Nov 16, 2020 - Nov 17, 2020 |
Boston, MA United States of America |
| Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions |
Nov 16, 2020 - Nov 17, 2020 |
Boston, MA United States of America |
| Introduction to Medical Combination Products |
Nov 18, 2020 - Nov 20, 2020 |
Boston, MA United States of America |
| Understanding & Implementing New EU Clinical Trial Regulation & GDPR |
Dec 10, 2020 - Dec 11, 2020 |
Malvern, PA United States of America |
