Home 2026 AMMI MEDTECH PROFESSIONAL CERTIFICATION PROGRAMME Posted on Sep 4, 2026Oct 13, 2026 Author admin 19 October 2026 to 17 December 2026: Medtech Professional Certificate in Quality Assurance (QA-Hybrid-3) ... Posted on Sep 4, 2026Oct 13, 2026 Author admin 22 October 2026 to 21 December 2026: Medtech Professional Certificate in Manufacturing Excellence (ME-Hybrid-3) ... 2026 AMMI PUBLIC TRAINING Posted on Jan 18, 2026Oct 13, 2026 Author Melissa 19 – 20 October 2026: Medical Device Quality System: ISO 13485:2016 & US FDA Quality Management System Regulation ... Posted on Jan 18, 2026Oct 13, 2026 Author 26 – 27 October 2026: Software Validation Requirements and Excel Spreadsheet Validation ... Posted on May 10, 2026Oct 13, 2026 Author 2 – 3 November 2026: Risk Management for Medical Devices (ISO 14971:2019 / EN ISO 14971:2019/A11:2021) ... Posted on May 12, 2026Oct 13, 2026 Author Melissa 16 – 17 November 2026: ISO 13485:2016 Quality Management System ... Posted on May 12, 2026Oct 13, 2026 Author 18 – 19 November 2026: Failure Mode and Effects Analysis (FMEA) in Medical Device Manufacturing ... Posted on May 12, 2026Oct 13, 2026 Author 20 November 2026: Effective Root Cause Analysis ... Posted on May 12, 2026Oct 13, 2026 Author Melissa 30 November – 1 December 2026: ISO 13485:2016 Internal Audit ... Posted on May 12, 2026Oct 13, 2026 Author 30 November – 1 December 2026: Medical Device Manufacturing Process Validation ... Posted on May 12, 2026Oct 13, 2026 Author 2 – 3 December 2026: NCR/ CAPA/ Complaint Handling ... Posted on May 21, 2026Oct 13, 2026 Author admin 14 – 15 December 2026: FDA QSR to QMSR: Understanding FDA’s New Requirements & Inspection Expectation ... Posted on May 21, 2026Oct 13, 2026 Author 16 – 17 December 2026: Medical Device Single Audit Program ... Posted on May 21, 2026Oct 13, 2026 Author 21 – 22 December 2026: EU Medical Device Regulation (EU MDR 2017/745) ... 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 Sep 4, 2026Oct 13, 2026 Author admin 19 October 2026 to 17 December 2026: Medtech Professional Certificate in Quality Assurance (QA-Hybrid-3) ...
Posted on Sep 4, 2026Oct 13, 2026 Author admin 22 October 2026 to 21 December 2026: Medtech Professional Certificate in Manufacturing Excellence (ME-Hybrid-3) ...
Posted on Jan 18, 2026Oct 13, 2026 Author Melissa 19 – 20 October 2026: Medical Device Quality System: ISO 13485:2016 & US FDA Quality Management System Regulation ...
Posted on Jan 18, 2026Oct 13, 2026 Author 26 – 27 October 2026: Software Validation Requirements and Excel Spreadsheet Validation ...
Posted on May 10, 2026Oct 13, 2026 Author 2 – 3 November 2026: Risk Management for Medical Devices (ISO 14971:2019 / EN ISO 14971:2019/A11:2021) ...
Posted on May 12, 2026Oct 13, 2026 Author Melissa 16 – 17 November 2026: ISO 13485:2016 Quality Management System ...
Posted on May 12, 2026Oct 13, 2026 Author 18 – 19 November 2026: Failure Mode and Effects Analysis (FMEA) in Medical Device Manufacturing ...
Posted on May 12, 2026Oct 13, 2026 Author Melissa 30 November – 1 December 2026: ISO 13485:2016 Internal Audit ...
Posted on May 12, 2026Oct 13, 2026 Author 30 November – 1 December 2026: Medical Device Manufacturing Process Validation ...
Posted on May 21, 2026Oct 13, 2026 Author admin 14 – 15 December 2026: FDA QSR to QMSR: Understanding FDA’s New Requirements & Inspection Expectation ...
Posted on May 21, 2026Oct 13, 2026 Author 16 – 17 December 2026: Medical Device Single Audit Program ...
Posted on May 21, 2026Oct 13, 2026 Author 21 – 22 December 2026: EU Medical Device Regulation (EU MDR 2017/745) ...