Newsletter | May 3, 2025

05.03.25 -- April's Most Popular Articles & Solutions

FEATURED EDITORIAL

The Future Of Medical Device Labeling Is Here

Medical device labels that lack information or contain inaccurate information may lead to product recalls or delays in product release.

Key QMS Considerations For Your Medical Device Startup

A quality management system (QMS) can often become bloated and unwieldy. This expert helps you understand key QMS basics and provides information.

Navigating The 2025 Medtech Regulatory Landscape In Switzerland And The U.K.

Switzerland is working toward reestablishing its relationship with the EU while exploring new avenues. Meanwhile, the U.K. is still rebuilding its regulatory framework post-Brexit.

TOP INDUSTRY INSIGHTS

Ophthalmic Delivery: Testing Drugs And Devices For Compliance

Explore ophthalmic drug and device testing, focusing on regulatory and patient compliance, including design considerations, testing methodologies, safety, and efficacy for medical device development.

Streamlining The Path To Market For Generic Drug-Device Combinations

Developing g-DDCPs is a complex and time-consuming process. By using a risk-based approach, manufacturers can streamline the development process and bring g-DDCPs to market more quickly.

Why Engineers Water Down Part Design

Discover why designing for manufacturability shouldn't mean settling for less, but rather striving for innovation with every micron.

TOP RESOURCES

HP Series Disc Pump

Meeting Annex 1: A Proactive Approach To Regulatory Compliance

Excel IV: An Evolving Market Affirms The Value Of An Established Offering

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