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Medical Tubing & Extrusion Experts Offer Perspectives on Industry
Supplying Sustainable Surfaces for Medical Device Coating and Finishing
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Reprieve Cardiovascular Emerges From Stealth Mode With $42M Financing
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Encore Medical Device Repair Introduces Robotic Remanufacturing and Sustainability Program at HSPA
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Medical Tubing & Extrusion Experts Offer Perspectives on Industry
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A Matter of Fact for Medical Device Materials
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FDA Releases Draft Guidance to Enhance Breast Implant Safety Information
FDA recommends including a boxed warning and other elements in breast implant labeling.
U.S. Food and Drug Administration
10.28.19
Contract Manufacturing
An Extension of Reach: A Discussion of Full-Service Outsourcing
OEMs recognize outsourcing service providers as opportunities for cutting costs and improving time to market while maintaining quality of product.
Sean Fenske, Editor-in-Chief
05.01.19
5 Questions Industry Professionals Should Ask About the EU MDR Rollout
As the May 2020 deadline approaches, the medical device industry must prepare for far-reaching changes.
Online Exclusives
Mike Edwards, Director of Product Management, Sparta Systems
01.04.19
Software & IT
Mistake-Proofing Production for Medical Device Manufacturing
Leveraging cloud-based and connected tools with eDHRs can significantly enhance a company’s quality program.
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Anca Thompson, SVP & Chief Quality Officer, Sanmina Corporation
12.18.18
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Implant Forward Thinking into Medical Device Supply Chains
New technologies enable medtech manufacturers to maintain a more efficient system.
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Josh Cannon, Director of Global Healthcare Strategy, UPS
06.30.17
Comparing cGMP Pharma vs. Device: Subpart A – General Provisions
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James A. Dunning, Owner, QPC Services LLC
06.06.17
Software & IT
FDB Launches FDB Prizm Medical Device Knowledge Platform
Platform brings clarity to medical device information within healthcare supply chain and clinical information systems.
Business Wire
02.17.17
R&D & Design
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Testing
5 New FDA Draft Guidances Issued for Medical Devices and Diagnostics
The proposed guidelines are now open for a 90-day public comment period.
Stephen Rapundalot, MichBio
08.01.16
Contract Manufacturing
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Materials
Combatting Counterfeiting in Medtech
Are OEMs and the FDA taking the necessary steps to deal with the problem?
Online Exclusives
Barry McDonogh, Vice President of Business Development, TruTag Technologies Inc.
05.05.16
FDA Narrows ‘Convenience Kit’ Definition for UDI Labeling
Update creates stricter interpretation of the term for UDI labeling and data submission requirements.
AAMI
01.06.16
Software & IT
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Testing
CDRH Seeks Increased Funding for Expanded Inspections, National Unique Device Identifier System
Device division of FDA asks for $384,815,000 in budget request, up $16,473,000 from last year.
Editor
02.03.10
Software & IT
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Testing
CDRH Seeks Increased Funding for Expanded Inspections, National Unique Device Identifier System
Device division of FDA asks for $384,815,000 in budget request, up $16,473,000 from last year.
Editor
02.03.10
Breaking News
Reprieve Cardiovascular Emerges From Stealth Mode With $42M Financing
Wearable Neuromodulation System for Urinary Incontinence Makes its Debut
Clinical Data Support Early Detection Ability of IR-MED's Pressure Injury Device
FineHeart Widens FlowMaker's International IP Protection
Encore Medical Device Repair Introduces Robotic Remanufacturing and Sustainability Program at HSPA
View Breaking News >
CURRENT ISSUE
April 2024
Medical Tubing & Extrusion Experts Offer Perspectives on Industry
Creating Sustainable Surfaces in Med Device Coating and Finishing
Man & Machine: Artificial Intelligence's Impact on Medtech
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