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  Will Consumer Electronics cause Medical Device Obsolescence?

  Will consumer electronics engulf the medical device development community, making rigorous testing and risk mitigation processes obsolete?

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  Faster Market Access for Less: Medical Device Single Audit Program (MDSAP)

  MDSAP enables Medical Device companies to save in Registrar’s fees, eliminate duplication of inspections and gain faster access to markets.

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  Re-use IVD Verification Test Equipment in Optics Manufacturing QC

  Reduce costs by reusing IVD Verification Test equipment for verification of optical components as part of manufacturing quality control.

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  Describing StarFish: Client satisfaction

  Results of StarFish client satisfaction survey with a large group that included customers and prospects using one word descriptions.

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  How to write a Medical Device Quality Manual (3 simple rules)

  Regulatory affairs expert explains how to write a best practice ISO 9000 Medical Device Quality Manual using 3 simple rules.

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  Electro-Medical Device Basic Safety Learning Lab Highlights

  Highlights from Day 1 of Learning Lab event at Boston BIOMEDevice on electro-medical device basic safety and achieving compliance with 60601.

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  Six ways to better manage and communicate medical device project relationships

  Six ways to manage and communicate medical device project relationships without losing the essence of the development innovation or wasting money.

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  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.

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  5 Top Annual Plan Medical Device Design and Development Process Improvement Recommendations

  Medical Device Design and Development Process Improvement for Annual Plan: limit improvement efforts, measure them regularly, succeed.

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