Strengthening Supplier Assessment in Medical Devices: Best Practices for Quality, Compliance, and Risk Mitigation

by Syrma Johari MedTech | Oct 23, 2025 | Blog

In today’s high-stakes MedTech landscape, your supplier network directly reflects your product integrity, regulatory posture, and time-to-market reliability. For manufacturers of Class II and III devices, supplier non-conformance can trigger far more than a CAPA. It...

Global Regulatory Submissions for Medical Devices

by Syrma Johari MedTech | Oct 16, 2025 | Blog

A practical guide to navigate complex global approval pathways for MedTech companies. Access the Full Guide Delayed time-to-market can translate directly into lost market revenue. Navigating global regulatory submissions has become a complex challenge for MedTech...

Syrma Johari MedTech Wins “Service Provider of the Year” at ET Healthcare Awards 2025

by Syrma Johari MedTech | Sep 8, 2025 | News and Events

We are thrilled to announce a significant milestone for Syrma Johari MedTech—winning the “Service Provider of the Year – Medical Supplies” at the ET Healthcare Awards 2025! This accolade is testament to our dedication in driving innovation, fostering resilience,...

Medical Device Contract Manufacturing: How to Choose the Right Partner

by Syrma Johari MedTech | Jul 8, 2025 | Blog

Medical device original equipment manufacturers (OEMs) are relying more than ever on contract manufacturing organizations (CMOs) to manage complex and capital-intensive manufacturing. Choosing the right medical device contract manufacturer is one of the most strategic...

Outsourcing Complaint Handling of Medical Devices? Regulatory Risks and How to Stay in Control

by Syrma Johari MedTech | Jun 16, 2025 | Blog

The medical device industry is an arena where patient safety, ethical responsibility, and precision engineering converge. High-stakes medical innovation demands rigorous compliance and intense regulatory scrutiny. Therefore, a single complaint can trigger a cascade of...