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How USA Medical Device companies can take advantage of ‘Make in India’?

by Syrma Johari MedTech | Dec 13, 2022 | Blog

Overview The Global Medical Device Contract Manufacturing Market is valued at USD 149.4 billion in 2029 from USD 78.9 billion in 2024 at a CAGR of 11.4% (source: Markets and Markets). The current market size of the medical devices industry in India is estimated at $11...

Wound Healing Devices: Emerging Technologies & Trends

by Syrma Johari MedTech | Dec 2, 2022 | Blog

Overview The significant rise in the number diabetic patients and acute wound cases across the globe has led to spike in demand for wound healing medical devices. The global wound care devices market size was valued at $2.19 Bn in 2019 & is projected to reach...

Supplier Qualification Process in Medical Device Manufacturing

by Syrma Johari MedTech | Nov 30, 2022 | Blog

A Medical Device is as good as its parts, this eventually makes supplier qualification process extremely important in Medical Device Design & Development. FDA 21 CFR 820.50 and ISO 13485:2016 Section 7.4 highlights major requirements for purchasing controls and...

Medical Device CAPA Process : Importance, benefits and implementation

by Syrma Johari MedTech | Nov 30, 2022 | Blog

A Medical Device Contract Manufacturing Organization is never at rest. With diversity of projects from different segments of Medical Device Industry, the possibilities of errors, risks, and upgrades are infinite. Every new project comes with its challenges and...

Medical Device Labeling: Importance, Do’s & Don’ts

by Syrma Johari MedTech | Sep 30, 2022 | Blog

A simple purchase decision for a regular use commodity is often influenced by the information printed on the product label. A Medical Device or Product is a high-risk commodity. For such products or devices labeling & packaging plays a crucial role in the final...
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Recent Posts

  • Syrma Johari MedTech Wins MedTech CDMO of the Year – Diagnostics & IVD
  • EU MDR Compliance Slowing Your MedTech Pipeline? Lessons from Real-World Case Studies
  • Quality Management for PCB Assembly (PCBA) in Complex Medical Devices: From Design to Deployment
  • Contract Manufacturing of Medical Devices: Through a Quality and Regulatory Lens
  • Regulatory Compliance for Energy-Based Aesthetic Devices: A Comprehensive Guide
  • Top 8 Fluorescence Immunoassay Technology Trends to Know
  • QARA-Centric Manufacturing: Embedding Regulatory Compliance into Every Stage of Medical Device Manufacturing
  • Tariff Engineering for Medical Devices: A Strategic Approach to Cost Optimization
  • Beyond Tariff Waves: Building Enduring Medtech Supply Chains – Part One
  • In Vitro Diagnostics (IVD) Growth & Trends: Clinical Impact Meets Commercial Opportunity
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