-
Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485 (Dec22)
December 12 to 16, 2022
Register
-
HTM Live!: If 85% of scope repairs are preventable - why spend so much?
January 10, 2023 12:00 AM to 12:00 AM
Register
-
Industrial Sterilization for Medical Devices (Jan23)
January 17 to 20, 2023
Register
-
Risk-Based Computer Software Assurance Approach for PPQS (January 2023)
January 24 to 26, 2023
Register
-
Integrating Risk Management to the Product Life Cycle (Feb23)
February 1 to 3, 2023
Register
-
Corrective & Preventive Actions, Requirements and Industry Practices (Feb23)
February 6 to 7, 2023
Register
-
Radiation Sterilization for Medical Devices (Feb23)
February 7 to 10, 2023
Register
-
Medical Device Cybersecurity 101 for HTM Professionals (Feb 2023)
February 7 to 9, 2023
Register
-
Design Control Requirements - Integrating the Quality System Regulation (Feb23)
February 15 to 17, 2023
Register
-
Introduction to Combination Products: A Risk-Based Approach
February 21 to 23, 2023
Register
-
HTMLive!: Getting to Know ACI & the Benefits of Certification (Feb2022)
February 21, 2023 12:00 AM to 12:00 AM
Register
-
Applying Control Charts for Visualizing and Detecting Trends (February 2023)
February 22, 2023 12:00 AM to 12:00 AM
Register
-
Ethylene Oxide Sterilization for Medical Devices (Mar23)
March 7 to 10, 2023
Register
-
HTM Live!: Maximize your CMMS to meet Regulatory Requirements
March 7, 2023 12:00 AM to 12:00 AM
Register
-
Human Factors for Medical Devices (Mar23)
March 14 to 16, 2023
Register
-
Medical Device Software Validation (Mar23)
March 21 to 23, 2023
Register
-
FMEA Without Tears (March 2023)
March 24, 2023 12:00 AM to 12:00 AM
Register
-
Navigating 510k & DeNovo Requirements (Mar23)
March 28 to 31, 2023
Register
-
CBET Study Course Online Spring 2023
April 3 to 26, 2023
Register
-
Process Validation Requirements & Industry Practices (Apr23)
April 4 to 6, 2023
Register
