Available Courses

Results (32)




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)