In the rapidly evolving healthcare landscape, medical devices play a pivotal role in enhancing patient care and improving health outcomes. The road to getting these devices from concept to patient use ...

Dublin, Jan. 30, 2025 (GLOBE NEWSWIRE) -- The "Verification and Validation - Product, Equipment/Process, Software and QMS" training has been added to ResearchAndMarkets.com's offering. This seminar ...

Overview: This course provides regulatory/quality professionals, manufacturing engineers, and process development engineers with the knowledge and skills needed to comply with the process validation ...

Medical device equipment manufacturers work in an environment where product quality isn't just a competitive advantage, it's a regulatory necessity with direct implications for patient safety. As ...

Dublin, Sept. 22, 2025 (GLOBE NEWSWIRE) -- The "US FDA Medical Device Quality System (QSR) Compliance: Design Controls, Verification & Validation (Oct 27th - Oct 28th, 2025)" training has been added ...

Medical Device Validation & Verification Market is witnessing a transformative growth phase-propelled by regulatory rigor, technological complexity. US, NY, UNITED STATES, August 6, 2025 /EINPresswire ...

DUBLIN--(BUSINESS WIRE)--The "Understanding FDA Design Verification and Validation Requirements for Medical Devices" webinar has been added to ResearchAndMarkets.com's offering. This webinar will help ...

Averna's Matt Thompson shares strategies to avoid common traps when transitioning medical devices from R&D to manufacturing.

Shashank Murali is a Quality Assurance professional based in Minneapolis, Minnesota, with more than eight years of experience in the medical device technology area.

(MENAFN- GlobeNewsWire - Nasdaq) This seminar offers medical device manufacturers the opportunity to enhance efficiency and compliance by applying Lean Documentation and Lean Configuration principles.