White Papers

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.
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.