Available Courses

Results (46)




Course Title Course Date Location
QbD - Product & Process Optimization using Design of Experiments Nov 22, 2017 - Nov 24, 2017 Berlin, Germany
Design Control for Medical Device Professionals Nov 28, 2017 - Nov 29, 2017 Malvern, PA United States
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Nov 30, 2017 - Dec 01, 2017 Malvern, PA United States
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Dec 04, 2017 - Dec 06, 2017 Malvern, PA United States
Computer System Validation Dec 07, 2017 - Dec 08, 2017 Los Angeles, CA United States
Effective Document Management for Pharma, Biotech & Medical Device Dec 11, 2017 - Dec 12, 2017 Berlin, Germany
Understanding & Implementing New EU Clinical Trial Regulation Dec 11, 2017 - Dec 12, 2017 Malvern, PA United States
Writing Effective SOP and Other Process Documents Dec 13, 2017 - Dec 14, 2017 Berlin, Germany
Biostatistics for Non-Statisticians Jan 22, 2018 - Jan 24, 2018 Los Angeles, CA United States
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Jan 22, 2018 - Jan 23, 2018 Los Angeles, CA United States
Introduction to Medical Combination Products Jan 24, 2018 - Jan 26, 2018 Los Angeles, CA United States
Understanding & Implementing New EU Clinical Trial Regulation Jan 25, 2018 - Jan 26, 2018 Los Angeles, CA United States
Effective Document Management for Pharma, Biotech & Medical Device Feb 01, 2018 - Feb 02, 2018 Los Angeles, CA United States
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Feb 05, 2018 - Feb 06, 2018 Los Angeles, CA United States
Overview of FDA Regulatory Compliance for Medical Devices Feb 05, 2018 - Feb 06, 2018 Malvern, PA United States
Selecting and Managing CROs Feb 05, 2018 - Feb 06, 2018 Los Angeles, CA United States
Clinical Trial Design For Medical Devices™ Feb 07, 2018 - Feb 08, 2018 Malvern, PA United States
Drug Marketing & Advertising of Pharmaceutical & Medical Devices Feb 07, 2018 - Feb 08, 2018 Malvern, PA United States
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Feb 07, 2018 - Feb 08, 2018 Los Angeles, CA United States
Writing Effective SOP and Other Process Documents Feb 07, 2018 - Feb 08, 2018 Los Angeles, CA United States
Auditing and Qualifying Suppliers and Vendors Mar 01, 2018 - Mar 02, 2018 Boston, MA United States
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Mar 01, 2018 - Mar 02, 2018 Malvern, PA United States
FDA Inspections - What Regulators Expect and How to Prepare Mar 05, 2018 - Mar 06, 2018 Los Angeles, CA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Mar 07, 2018 - Mar 09, 2018 Los Angeles, CA United States
Project Management for Medical Device Product Development Mar 08, 2018 - Mar 09, 2018 Los Angeles, CA United States
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Mar 12, 2018 - Mar 13, 2018 Malvern, PA United States
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Mar 12, 2018 - Mar 13, 2018 Berlin, Germany
Introduction to Medical Combination Products Mar 14, 2018 - Mar 16, 2018 Berlin, Germany
QbD - Product & Process Optimization using Design of Experiments Mar 19, 2018 - Mar 21, 2018 Boston, MA United States
Understanding Sterilization Methods for Products and Devices Mar 21, 2018 - Mar 22, 2018 Malvern, PA United States
Biostatistics for Non-Statisticians Mar 26, 2018 - Mar 28, 2018 Berlin, Germany
Design Control for Medical Device Professionals Apr 09, 2018 - Apr 10, 2018 Los Angeles, CA United States
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Apr 11, 2018 - Apr 12, 2018 Los Angeles, CA United States
Computer System Validation Apr 12, 2018 - Apr 13, 2018 Berlin, Germany
Introduction to Effective Medical Writing Apr 23, 2018 - Apr 24, 2018 Malvern, PA United States
Medical Device Auditing Course: ISO 19011:2011 Framework Apr 23, 2018 - Apr 25, 2018 Los Angeles, CA United States
Heating, Ventilation & A/C in a Regulated Environment Apr 25, 2018 - Apr 27, 2018 Los Angeles, CA United States
Technical Writing for Pharma, Biotech and Med Devices Apr 25, 2018 - Apr 27, 2018 Malvern, PA United States
Medical Device Auditing Course: EN ISO 13485: 2016 Changes Apr 25, 2018 - Apr 27, 2018 Los Angeles, CA United States
Integration of Risk Management Principles and Activities into the Quality System May 14, 2018 - May 15, 2018 Malvern, PA United States
Medical Device Process Validation Training for Professionals May 16, 2018 - May 18, 2018 Malvern, PA United States
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions May 21, 2018 - May 22, 2018 Malvern, PA United States
Writing Effective SOP and Other Process Documents May 21, 2018 - May 22, 2018 Boston, MA United States
Introduction to Medical Combination Products May 23, 2018 - May 25, 2018 Malvern, PA United States
Design Control for Medical Device Professionals May 29, 2018 - May 30, 2018 Berlin, Germany
Design Validation, Verification, and Risk Analysis for Medical Device Professionals May 31, 2018 - Jun 01, 2018 Berlin, Germany