Available Courses

Results (30)




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
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
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Jun 17, 2020 - Jun 19, 2020 Boston, MA 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