Home CLICK HERE FOR MORE INFO CLICK HERE FOR MORE INFORMATION 2026 AMMI MEDTECH PROFESSIONAL CERTIFICATION PROGRAMME Posted on Feb 24, 2026Mar 12, 2026 Author Wendy 31 March 2026 to 26 June 2026: Medtech Professional Certificate in Quality Assurance (QA-Penang-1) ... Posted on Feb 24, 2026Apr 2, 2026 Author Wendy 13 April 2026 to 3 July 2026: Medtech Professional Certificate in Manufacturing Excellence (ME-Penang-1) ... 2026 AMMI PUBLIC TRAINING Posted on Jan 18, 2026May 13, 2026 Author Wendy 27 – 28 July 2026: FDA QSR to QMSR: Understanding FDA’s New Requirements & Inspection Expectation ... Posted on Jan 18, 2026May 13, 2026 Author Wendy 29 July 2026: Effective Root Cause Analysis ... Posted on Jan 18, 2026Jun 16, 2026 Author Wendy 5 – 6 August 2026: EU Medical Device Regulation (EU MDR 2017/745) ... Posted on Jan 18, 2026Jun 16, 2026 Author Wendy 17 – 18 August 2026: Risk Management for Medical Devices (ISO 14971:2019 / EN ISO 14971:2019/A11:2021) ... Posted on Jan 18, 2026Jun 7, 2026 Author Wendy 7 – 8 September 2026: NCR/ CAPA/ Complaint Handling ... Posted on Jan 18, 2026Jun 7, 2026 Author Wendy 21 September 2026: Effective Root Cause Analysis ... Posted on Jan 18, 2026Jul 2, 2026 Author Melissa 28 – 29 September 2026: Medical Device Design Control ... Posted on Jan 18, 2026Jul 2, 2026 Author Wendy 12 – 13 October 2026: Medical Device Change Control ... Posted on Jan 18, 2026Jun 7, 2026 Author Wendy 19 – 20 October 2026: Medical Device Quality System: ISO 13485:2016 & US FDA Quality Management System Regulation ... Posted on Jan 18, 2026Jun 9, 2026 Author Melissa 21 – 22 October 2026: ISO 13485:2016 Internal Audit ... Posted on May 12, 2026Jul 24, 2026 Author Wendy 26 – 27 October 2026: Software Validation Requirements and Excel Spreadsheet Validation ... Posted on May 12, 2026Jul 24, 2026 Author Melissa 16 – 17 November 2026: ISO 13485:2016 Quality Management System ... Posted on May 12, 2026Jun 7, 2026 Author Wendy 30 November – 1 December 2026: Medical Device Manufacturing Process Validation ... Posted on May 13, 2026Jul 15, 2026 Author Wendy 16 – 17 December 2026: Medical Device Single Audit Program ... FOR MORE TRAINING COURSES, CLICK HERE CLICK HERE Advertisements 2026 TRAINING WISH LIST You are invited to submit your 2026 training wish list and we will turn the most requested courses into public training classes for you! Submit Your Wish List Here
Posted on Feb 24, 2026Mar 12, 2026 Author Wendy 31 March 2026 to 26 June 2026: Medtech Professional Certificate in Quality Assurance (QA-Penang-1) ...
Posted on Feb 24, 2026Apr 2, 2026 Author Wendy 13 April 2026 to 3 July 2026: Medtech Professional Certificate in Manufacturing Excellence (ME-Penang-1) ...
Posted on Jan 18, 2026May 13, 2026 Author Wendy 27 – 28 July 2026: FDA QSR to QMSR: Understanding FDA’s New Requirements & Inspection Expectation ...
Posted on Jan 18, 2026Jun 16, 2026 Author Wendy 5 – 6 August 2026: EU Medical Device Regulation (EU MDR 2017/745) ...
Posted on Jan 18, 2026Jun 16, 2026 Author Wendy 17 – 18 August 2026: Risk Management for Medical Devices (ISO 14971:2019 / EN ISO 14971:2019/A11:2021) ...
Posted on Jan 18, 2026Jun 7, 2026 Author Wendy 7 – 8 September 2026: NCR/ CAPA/ Complaint Handling ...
Posted on Jan 18, 2026Jul 2, 2026 Author Melissa 28 – 29 September 2026: Medical Device Design Control ...
Posted on Jan 18, 2026Jul 2, 2026 Author Wendy 12 – 13 October 2026: Medical Device Change Control ...
Posted on Jan 18, 2026Jun 7, 2026 Author Wendy 19 – 20 October 2026: Medical Device Quality System: ISO 13485:2016 & US FDA Quality Management System Regulation ...
Posted on Jan 18, 2026Jun 9, 2026 Author Melissa 21 – 22 October 2026: ISO 13485:2016 Internal Audit ...
Posted on May 12, 2026Jul 24, 2026 Author Wendy 26 – 27 October 2026: Software Validation Requirements and Excel Spreadsheet Validation ...
Posted on May 12, 2026Jul 24, 2026 Author Melissa 16 – 17 November 2026: ISO 13485:2016 Quality Management System ...
Posted on May 12, 2026Jun 7, 2026 Author Wendy 30 November – 1 December 2026: Medical Device Manufacturing Process Validation ...
Posted on May 13, 2026Jul 15, 2026 Author Wendy 16 – 17 December 2026: Medical Device Single Audit Program ...