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USA Health Panel has made anxiety level checks mandatory for US Population! Johari’s Possible Solution…

by Syrma Johari MedTech | Sep 27, 2022 | Blog

With a significant rise in anxiety levels in the US population, United Nations Human Health & Service department-led Health panel has come up with an initiative to make mental health & anxiety checks mandatory for all adults up to 65 years of age. An estimated...

Is Post Market Design Enhancement a roadblock for your Medical Device Market Sustainability?

by Syrma Johari MedTech | Sep 24, 2022 | Blog

Medical Device Development is a highly regulated task involving different talents including Engineering, Manufacturing, Designing, Regulatory& Quality, Sales & Marketing. Medical Device Contract Manufacturing unit needs the joint efforts of all these...

Pain Relief by Electrotherapy: A brief history & Useful Indications

by Syrma Johari MedTech | Sep 19, 2022 | Blog

Discovery of Electrotherapy was a serendipity. You don’t believe it? We’ll tell you how! A student at the University of Halle in Germany discovered that electricity caused an improvement in paralysis. Electricity improved heart rate, sleep, and induced...

Understanding Bill of Materials (BOM) for Medical Devices: A Comprehensive Guide

by Syrma Johari MedTech | Sep 16, 2022 | Blog

What is BOM (Bill of Material)?  A comprehensive list comprising prices involved in the development of a medical device is referred to as the Bill of Material (BOM). This may include Raw Materials, Assemblies, Sub-Assemblies, Work Force, Machinery, and Quantities...

How to Bridge the Gap between Market Research and Medical Device Development Team?

by Syrma Johari MedTech | Sep 8, 2022 | Blog

Medical Device Development is a highly regulated task involving multiple stages and different talents. The marketers in the MedTech firms are the first ones to interact with a new product idea. From day one when the discussion around a project begins to the time it...
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Recent Posts

  • Strengthening Supplier Assessment in Medical Devices: Best Practices for Quality, Compliance, and Risk Mitigation
  • Global Regulatory Submissions for Medical Devices
  • Syrma Johari MedTech Wins “Service Provider of the Year” at ET Healthcare Awards 2025
  • Medical Device Contract Manufacturing: How to Choose the Right Partner
  • Outsourcing Complaint Handling of Medical Devices? Regulatory Risks and How to Stay in Control
  • Case Study – Cost-Effective, Scalable Manufacturing for a Life-Saving IVD Platform
  • 7 Key Questions to Ask Before Choosing a Medical Device Contract Manufacturer
  • Why Proactive Component Obsolescence Management Is Critical for Medical Device Manufacturers
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