• 

  Using Proven Process for Medical Device Success: Part 1 – IP to Reimbursement Strategy

  Medical Device Pathfinder process for Intellectual Property, Consumables Strategy, Value Chain and Margin, and Reimbursement.

• 

  Avoid Waste Preparing for Medical Device Regulatory Requirements

  The best way to avoid waste is to consider medical device regulatory requirements at a project outset.

• 

  RoHS 2 and Medical Devices: Compliance Overview

  RoHS 2 and Medical Devices impact design and manufacture. Failure to meet requirements could result in product recalls.

• 

  Reader Favorites: 10 Most Read StarFish Medical Device Blogs of 2013

  Reader Favorites: 10 Most Read StarFish Medical Device Blogs of 2013. From FDA Guidelines to EMS pre-screening to Medical Device Margins.

• 

  How to Handle Medical Device Risk Management and the change from ALARP to AFAP

  Medical Device Risk Management ALARP to AFAP, the Directive and Standard, implications and how to handle the situation.

• 

  3 Golden Rules for Managing Subcontractors

  Tips for managing subcontractors —especially in regulatory submissions, EMC testing, injection moulding, and rapid prototyping.

• 

  Planning, Input and Architecture Tips for Medical Device Design Documentation

  Three medical device design documentation tips for Planning, Input and Architecture when developing early stage medical devices.

• 

  Toyota, SOUP, and Medical Device Software of Unknown Provenance

  Ways to safely handle Medical Device Software of Unknown Provenance and third party code in Medical Device Development.

• 

  5 Tips for FDA 510(k) Medical Device Regulatory Clearance

  FDA 510(k) medical device submission tips and advice: being adequately prepared is essential for a smooth submission.

There are no posts to show