White Papers

IVD products whitepaper

Beyond Tariff Waves: Building Enduring MedTech Supply Chains – Part Two

This white paper outlines strategies for medical device companies to strengthen supply continuity and scale global manufacturing despite tariff pressures.

IVD products whitepaper

Leveraging Design for Manufacturing (DFM) to Streamline Electronic Medical Device Manufacturing

Design for Manufacturing (DFM) helps MedTech companies turn innovative designs into manufacturable and cost-efficient medical devices. Read the white paper.

IVD products whitepaper

From Due Diligence to Integration: The Strategic Role of Regulatory Affairs in MedTech Mergers & Acquisitions

Learn how regulatory affairs integration de-risks MedTech M&A. Download Syrma Johari MedTech’s whitepaper for due diligence and post-merger checklists.

IVD products whitepaper

From Lab to Market: A Tactical Blueprint to Scale IVD Products

Taking an in-vitro diagnostic (IVD) product from laboratory concept to commercial launch is a complex and high-risk process. The core operational challenge is transforming a promising prototype into a fully regulated, mass-manufactured product without encountering hurdles such as yield issues, material changes, single-supplier dependencies, or documentation breakdowns.

On Demand Webinar Navigating the Impact of Component Obsolescence in MedTech Manufacturing

Streamlining Medical Device PCB Assembly: Best Practices for Agility & High-Reliability PCBA

Medical PCBAs form the backbone of life-saving devices. Yet, challenges like soldering defects, delamination, improper coating, and manual documentation continue to impact yield, time-to-market, and compliance. This whitepaper is packed with real-world insights and proven practices for MedTech OEMs and contract manufacturers looking to level up their PCBA process.

USA Tariff

Navigating the 50% U.S. Tariff: Why India Remains a Strategic MedTech Manufacturing Partner

The 50% tariff on Indian medical device imports is reshaping how OEMs and procurement teams approach sourcing and cost management. This knowledge guide provides a clear framework for MedTech leaders to respond with confidence—offering strategies to optimize sourcing, control landed costs and build resilient global partnerships.

QARA Whitepaper

Unlocking Competitive Advantage through QARA Integration in Medical Device Manufacturing

This whitepaper explores how Quality Assurance and Regulatory Affairs (QARA) is shifting from a reactive compliance function to a strategic driver of innovation in MedTech contract manufacturing. By integrating QARA into product design and development, manufacturers can accelerate time-to-market, strengthen global compliance, and turn regulatory alignment into a competitive advantage.