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Course Title Course Date Location
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Jun 25, 2018 - Jun 26, 2018 Malvern, PA United States
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Jun 27, 2018 - Jun 28, 2018 Malvern, PA United States
Biostatistics for Non-Statisticians Jul 11, 2018 - Jul 13, 2018 Malvern, PA United States
Understanding & Implementing New EU Clinical Trial Regulation Aug 02, 2018 - Aug 03, 2018 Malvern, PA United States
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Aug 06, 2018 - Aug 08, 2018 Los Angeles, CA United States
Medical Writing When English Is Your Second Language Aug 06, 2018 - Aug 07, 2018 Malvern, PA United States
Writing Effective SOP and Other Process Documents Aug 08, 2018 - Aug 09, 2018 Malvern, PA United States
Design Control for Medical Device Professionals Aug 13, 2018 - Aug 14, 2018 Malvern, PA United States
Introduction to Effective Medical Writing Aug 13, 2018 - Aug 14, 2018 Los Angeles, CA United States
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Aug 15, 2018 - Aug 16, 2018 Malvern, PA United States
Technical Writing for Pharma, Biotech and Med Devices Aug 15, 2018 - Aug 17, 2018 Los Angeles, CA United States
Effective Document Management for Pharma, Biotech & Medical Device Aug 23, 2018 - Aug 24, 2018 Boston, MA United States
Project Management for Medical Device Product Development Sep 06, 2018 - Sep 07, 2018 Malvern, PA United States
Auditing and Qualifying Suppliers and Vendors Sep 13, 2018 - Sep 14, 2018 Malvern, PA United States
Computer System Validation Sep 13, 2018 - Sep 14, 2018 Malvern, PA United States
Overview of FDA Regulatory Compliance for Medical Devices Sep 17, 2018 - Sep 18, 2018 Malvern, PA United States
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Sep 24, 2018 - Sep 25, 2018 Malvern, PA United States
Introduction to Effective Medical Writing Sep 24, 2018 - Sep 25, 2018 Berlin, Germany
Introduction to Medical Combination Products Sep 26, 2018 - Sep 28, 2018 Malvern, PA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Sep 26, 2018 - Sep 28, 2018 Boston, MA United States
Technical Writing for Pharma, Biotech and Med Devices Sep 26, 2018 - Sep 28, 2018 Berlin, Germany
Understanding & Implementing New EU Clinical Trial Regulation Oct 04, 2018 - Oct 05, 2018 Boston, MA United States
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Oct 11, 2018 - Oct 12, 2018 Boston, MA United States
Auditing and Qualifying Suppliers and Vendors Oct 15, 2018 - Oct 16, 2018 Berlin, Germany
Biostatistics for Non-Statisticians Oct 15, 2018 - Oct 17, 2018 Boston, MA United States
Writing Effective SOP and Other Process Documents Oct 15, 2018 - Oct 16, 2018 Boston, MA United States
Selecting and Managing CROs Oct 17, 2018 - Oct 18, 2018 Boston, MA United States
Advanced Topics in Biostatistics for Non-Statisticians™ Oct 18, 2018 - Oct 19, 2018 Boston, MA United States
Clinical Trial Design For Medical Devices™ Oct 18, 2018 - Oct 19, 2018 Malvern, PA United States
Medical Device Process Validation Training for Professionals Oct 22, 2018 - Oct 24, 2018 Berlin, Germany
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Oct 25, 2018 - Oct 26, 2018 Berlin, Germany
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Nov 05, 2018 - Nov 06, 2018 Boston, MA United States
Medical Device Auditing Course: ISO 19011:2011 Framework Nov 05, 2018 - Nov 07, 2018 Malvern, PA United States
Drug Marketing & Advertising of Pharmaceutical & Medical Devices Nov 06, 2018 - Nov 07, 2018 Boston, MA United States
Overview of FDA Regulatory Compliance for Medical Devices Nov 06, 2018 - Nov 07, 2018 El Paso, TX United States
Medical Device Auditing Course: EN ISO 13485: 2016 Changes Nov 07, 2018 - Nov 09, 2018 Malvern, PA United States
Integration of Risk Management Principles and Activities into the Quality System Nov 12, 2018 - Nov 13, 2018 Los Angeles, CA United States
Medical Device Process Validation Training for Professionals Nov 14, 2018 - Nov 15, 2018 Los Angeles, CA United States
QbD - Product & Process Optimization using Design of Experiments Nov 26, 2018 - Nov 28, 2018 Berlin, Germany
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Dec 03, 2018 - Dec 05, 2018 Boston, MA United States
Computer System Validation Dec 06, 2018 - Dec 07, 2018 Los Angeles, CA United States
Project Management for Medical Device Product Development Dec 06, 2018 - Dec 07, 2018 El Paso, TX United States
Writing Effective SOP and Other Process Documents Dec 06, 2018 - Dec 07, 2018 Berlin, Germany
Introduction to Effective Medical Writing Dec 10, 2018 - Dec 11, 2018 Boston, MA United States
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Dec 11, 2018 - Dec 12, 2018 El Paso, TX United States
Technical Writing for Pharma, Biotech and Med Devices Dec 12, 2018 - Dec 14, 2018 Boston, MA United States
Design Control for Medical Device Professionals Jan 28, 2019 - Jan 29, 2019 El Paso, TX United States
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Jan 30, 2019 - Jan 31, 2019 El Paso, TX United States