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Course Title Course Date Location
Writing Effective SOP and Other Process Documents Feb 28, 2019 - Mar 01, 2019 Los Angeles, CA United States of America
Introduction to Medical Combination Products Mar 04, 2019 - Mar 06, 2019 Boston, MA United States of America
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Mar 07, 2019 - Mar 08, 2019 Boston, MA United States of America
FDA Inspections - What Regulators Expect and How to Prepare Mar 18, 2019 - Mar 19, 2019 Malvern, PA United States of America
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Mar 20, 2019 - Mar 21, 2019 El Paso, TX United States of America
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Mar 20, 2019 - Mar 22, 2019 Malvern, PA United States of America
Understanding & Implementing New EU Clinical Trial Regulation & GDPR Mar 27, 2019 - Mar 28, 2019 Malvern, PA United States of America
Technical Writing for Pharma, Biotech and Med Devices Apr 01, 2019 - Apr 03, 2019 Malvern, PA United States of America
Biostatistics for Non-Statisticians Apr 03, 2019 - Apr 05, 2019 London, United Kingdom
Clinical Trial Design For Medical Devices™ Apr 03, 2019 - Apr 04, 2019 Boston, MA United States of America
QbD - Product & Process Optimization using Design of Experiments Apr 03, 2019 - Apr 05, 2019 Boston, MA United States of America
Selecting and Managing CROs Apr 04, 2019 - Apr 05, 2019 Malvern, PA United States of America
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Apr 08, 2019 - Apr 10, 2019 Malvern, PA United States of America
Design Control for Medical Device Professionals Apr 08, 2019 - Apr 09, 2019 London, United Kingdom
Computer System Validation Apr 10, 2019 - Apr 11, 2019 Malvern, PA United States of America
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Apr 10, 2019 - Apr 11, 2019 London, United Kingdom
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Apr 24, 2019 - Apr 25, 2019 Boston, MA United States of America
Technical Writing for Pharma, Biotech and Med Devices Apr 29, 2019 - May 01, 2019 London, United Kingdom
Writing Effective SOP and Other Process Documents May 02, 2019 - May 03, 2019 London, United Kingdom
Integration of Risk Management Principles and Activities into the Quality System May 06, 2019 - May 07, 2019 Malvern, PA United States of America
Medical Device Process Validation Training for Professionals May 08, 2019 - May 10, 2019 Malvern, PA United States of America
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials May 09, 2019 - May 10, 2019 Malvern, PA United States of America
Advanced Blockchain Concepts for the Pharmaceutical and Medical Device Industries May 13, 2019 - May 14, 2019 Malvern, PA United States of America
Design Control for Medical Device Professionals May 13, 2019 - May 14, 2019 Malvern, PA United States of America
QbD - Product & Process Optimization using Design of Experiments May 13, 2019 - May 15, 2019 London, United Kingdom
Design Validation, Verification, and Risk Analysis for Medical Device Professionals May 15, 2019 - May 16, 2019 Malvern, PA United States of America
Auditing and Qualifying Suppliers and Vendors May 16, 2019 - May 17, 2019 London, United Kingdom
Computer System Validation May 20, 2019 - May 21, 2019 London, United Kingdom
Drug Marketing & Advertising of Pharmaceutical & Medical Devices May 21, 2019 - May 22, 2019 Malvern, PA United States of America
Auditing and Qualifying Suppliers and Vendors Jun 06, 2019 - Jun 07, 2019 Malvern, PA United States of America
Biostatistics for Non-Statisticians Jun 17, 2019 - Jun 19, 2019 Boston, MA United States of America
Overview of FDA Regulatory Compliance for Medical Devices Jun 19, 2019 - Jun 20, 2019 Boston, MA United States of America
Advanced Topics in Biostatistics for Non-Statisticians™ Jun 20, 2019 - Jun 21, 2019 Boston, MA United States of America
Qualifying, Management and Auditing of Contract Manufacturing Organizations Jul 10, 2019 - Jul 11, 2019 Los Angeles, CA United States of America
FDA Inspections - What Regulators Expect and How to Prepare Jul 15, 2019 - Jul 16, 2019 Los Angeles, CA United States of America
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Jul 17, 2019 - Jul 19, 2019 Los Angeles, CA United States of America
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Jul 17, 2019 - Jul 19, 2019 Los Angeles, CA United States of America
Introduction to Medical Combination Products Jul 22, 2019 - Jul 24, 2019 Los Angeles, CA United States of America
Technical Writing for Pharma, Biotech and Med Devices Jul 22, 2019 - Jul 24, 2019 Los Angeles, CA United States of America
Computer System Validation Jul 24, 2019 - Jul 25, 2019 Los Angeles, CA United States of America
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Jul 25, 2019 - Jul 26, 2019 Los Angeles, CA United States of America
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Aug 05, 2019 - Aug 06, 2019 Los Angeles, CA United States of America
Medical Devices: The New MDRs, EU Directives, Guidance, CE Marking and ISO Standard Certifications Aug 07, 2019 - Aug 08, 2019 Los Angeles, CA United States of America
Understanding & Implementing New EU Clinical Trial Regulation & GDPR Aug 19, 2019 - Aug 20, 2019 Boston, MA United States of America
Design Control for Medical Device Professionals Sep 16, 2019 - Sep 17, 2019 Los Angeles, CA United States of America
FDA Inspections - What Regulators Expect and How to Prepare Sep 16, 2019 - Sep 17, 2019 London, United Kingdom
Overview of FDA Regulatory Compliance for Medical Devices Sep 16, 2019 - Sep 17, 2019 Malvern, PA United States of America
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Sep 18, 2019 - Sep 19, 2019 Los Angeles, CA United States of America
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Sep 18, 2019 - Sep 20, 2019 London, United Kingdom
Effective Document Management for Pharma, Biotech & Medical Device Sep 23, 2019 - Sep 24, 2019 Malvern, PA United States of America
Writing Effective SOP and Other Process Documents Sep 25, 2019 - Sep 26, 2019 Malvern, PA United States of America
Auditing and Qualifying Suppliers and Vendors Oct 03, 2019 - Oct 04, 2019 Boston, MA United States of America
Clinical Trial Design For Medical Devices™ Oct 07, 2019 - Oct 08, 2019 Malvern, PA United States of America
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Oct 16, 2019 - Oct 17, 2019 Boston, MA United States of America
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
Drug Marketing & Advertising of Pharmaceutical & Medical Devices Oct 29, 2019 - Oct 30, 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
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
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
Technical Writing for Pharma, Biotech and Med Devices Dec 04, 2019 - Dec 06, 2019 Boston, MA United States of America
Qualifying, Management and Auditing of Contract Manufacturing Organizations Dec 12, 2019 - Dec 13, 2019 Malvern, PA United States of America
Writing Effective SOP and Other Process Documents Dec 12, 2019 - Dec 13, 2019 Boston, MA United States of America