Available Courses

Results (33)




Course Title Course Date Location
Design Control for Medical Device Professionals Aug 10, 2020 - Aug 11, 2020 Virtual (CDT),
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Aug 12, 2020 - Aug 13, 2020 Virtual (EDT),
Technical Writing for Pharma, Biotech and Med Devices Sep 09, 2020 - Sep 11, 2020 Virtual (EDT),
Effective Document Management for Pharma, Biotech & Medical Device Sep 14, 2020 - Sep 15, 2020 Virtual (EDT),
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Sep 14, 2020 - Sep 15, 2020 Virtual (PDT),
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Sep 21, 2020 - Sep 22, 2020 Virtual (EDT),
Auditing and Qualifying Suppliers and Vendors Sep 24, 2020 - Sep 25, 2020 Virtual (BST),
Overview of FDA Regulatory Compliance for Medical Devices Sep 24, 2020 - Sep 25, 2020 Virtual (PDT),
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Oct 05, 2020 - Oct 06, 2020 Virtual (BST),
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Oct 05, 2020 - Oct 07, 2020 Virtual (EDT),
Medical Device Process Validation Training for Professionals Oct 07, 2020 - Oct 09, 2020 Virtual (BST),
Biostatistics for Non-Statisticians Oct 07, 2020 - Oct 09, 2020 Virtual (EDT),
Design Control for Medical Device Professionals Oct 12, 2020 - Oct 13, 2020 Virtual (BST),
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Oct 14, 2020 - Oct 15, 2020 Virtual (BST),
Auditing and Qualifying Suppliers and Vendors Oct 15, 2020 - Oct 16, 2020 Virtual (PDT),
Selecting and Managing CROs Oct 15, 2020 - Oct 16, 2020 Virtual (EDT),
Clinical Trial Design For Medical Devices™ Oct 19, 2020 - Oct 20, 2020 Virtual (EDT),
Integration of Risk Management Principles and Activities into the Quality System Oct 19, 2020 - Oct 20, 2020 Virtual (EDT),
Medical Device Process Validation Training for Professionals Oct 21, 2020 - Oct 23, 2020 Virtual (EDT),
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Oct 21, 2020 - Oct 23, 2020 Virtual (PDT),
Qualifying, Management and Auditing of Contract Manufacturing Organizations Oct 22, 2020 - Oct 23, 2020 Virtual (PDT),
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Oct 22, 2020 - Oct 23, 2020 Virtual (EDT),
Medical Devices: The New MDRs, EU Directives, Guidance, CE Marking and ISO Standard Certifications Oct 26, 2020 - Oct 27, 2020 Virtual (EDT),
QbD - Product & Process Optimization using Design of Experiments Nov 09, 2020 - Nov 11, 2020 Virtual (EST),
Computer System Validation Nov 09, 2020 - Nov 10, 2020 Virtual (EST),
Design Control for Medical Device Professionals Nov 09, 2020 - Nov 10, 2020 Virtual (EST),
FDA Inspections - What Regulators Expect and How to Prepare Nov 09, 2020 - Nov 10, 2020 Virtual (PST),
Technical Writing for Pharma, Biotech and Med Devices Nov 11, 2020 - Nov 13, 2020 Virtual (EST),
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Nov 12, 2020 - Nov 13, 2020 Virtual (EST),
Marketing & Advertising of Pharmaceutical & Medical Devices Nov 16, 2020 - Nov 17, 2020 Virtual (EST),
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Nov 16, 2020 - Nov 17, 2020 Virtual (EST),
Introduction to Medical Combination Products Nov 18, 2020 - Nov 20, 2020 Virtual (EST),
Understanding & Implementing New EU Clinical Trial Regulation & GDPR Dec 10, 2020 - Dec 11, 2020 Virtual (EST),