| Course Title |
Course Date |
Location |
| Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries |
Oct 17, 2019 - Oct 18, 2019 |
Malvern, PA United States of America |
| Biostatistics for Non-Statisticians |
Oct 21, 2019 - Oct 23, 2019 |
Malvern, PA United States of America |
| Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies |
Oct 23, 2019 - Oct 25, 2019 |
Boston, MA United States of America |
| GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials |
Oct 24, 2019 - Oct 25, 2019 |
Boston, MA United States of America |
| Integration of Risk Management Principles and Activities into the Quality System |
Nov 04, 2019 - Nov 05, 2019 |
Los Angeles, CA United States of America |
| Technical Writing for Pharma, Biotech and Med Devices |
Nov 04, 2019 - Nov 06, 2019 |
London, United Kingdom |
| Introduction to Medical Combination Products |
Nov 06, 2019 - Nov 08, 2019 |
Boston, MA United States of America |
| Medical Device Process Validation Training for Professionals |
Nov 06, 2019 - Nov 08, 2019 |
Los Angeles, CA United States of America |
| Advanced Blockchain Concepts for the Pharmaceutical and Medical Device Industries |
Nov 07, 2019 - Nov 08, 2019 |
Los Angeles, CA United States of America |
| Writing Effective SOP and Other Process Documents |
Nov 07, 2019 - Nov 08, 2019 |
London, United Kingdom |
| Computer System Validation |
Nov 13, 2019 - Nov 14, 2019 |
Boston, MA United States of America |
| FDA Inspections - What Regulators Expect and How to Prepare |
Nov 18, 2019 - Nov 19, 2019 |
Boston, MA United States of America |
| Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy |
Nov 20, 2019 - Nov 22, 2019 |
Boston, MA United States of America |
| Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions |
Dec 02, 2019 - Dec 03, 2019 |
Boston, MA United States of America |
| Technical Writing for Pharma, Biotech and Med Devices |
Dec 04, 2019 - Dec 06, 2019 |
Boston, MA United States of America |
| Writing Effective SOP and Other Process Documents |
Dec 12, 2019 - Dec 13, 2019 |
Boston, MA United States of America |
| 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 |
Malvern, PA United States of America |
| 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 |
Malvern, PA United States of America |
| Overview of FDA Regulatory Compliance for Medical Devices |
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 |
| Computer System Validation |
Mar 30, 2020 - Mar 31, 2020 |
Malvern, PA 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 |
| 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 |
| Design Control for Medical Device Professionals |
Jun 08, 2020 - Jun 09, 2020 |
Los Angeles, CA United States of America |
| Design Validation, Verification, and Risk Analysis for Medical Device Professionals |
Jun 10, 2020 - Jun 11, 2020 |
Los Angeles, CA United States of America |
| Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies |
Jun 15, 2020 - Jun 17, 2020 |
Los Angeles, CA United States of America |
| Auditing and Qualifying Suppliers and Vendors |
Jun 25, 2020 - Jun 26, 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 |
