Addressing Common Pitfalls in Clinical Study Protocols: Practical Solutions and Best Practices
Published: May 13, 2025
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Five Mistakes to Avoid in Medical Device Clinical Trial Management and How to Fix Them
Published: May 6, 2025
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Top 6 Reasons Medical Device Proof-of-Concept Studies Fail
Published: April 30, 2025
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Rethinking Cytotoxicity: Do Cytotoxicity Results Predict In Vivo Outcomes?
Published: April 23, 2025
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Guide to Clinical Evaluation Reports (CER) for Medical Devices
Published: April 17, 2025
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Guide to Understanding FDA Preclinical Study Requirements for Medical Devices
Published: April 10, 2025
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The Newly Applied European Health Technology Assessment (HTA) Regulation: Implications for Medical Devices
Published: April 9, 2025
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ISO 10993-7 Primer: Testing for Ethylene Oxide Sterilization Residuals
Published: April 4, 2025
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Impact of FDA Changes on MedTech Research
Published: April 3, 2025
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FDA Real-World Evidence: What Does It Really Mean and How Does It Work?
Published: April 2, 2025
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Navigating the Regulatory Journey of Combination Products: A Focus on Material Characterization
Published: March 28, 2025
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FDA Premarket and Postmarket Medical Device Cybersecurity
Published: March 26, 2025
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PMCF Best Practices: Strategies for Notified Body Approval
Published: March 25, 2025
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Key Components of a Biological Evaluation Plan (BEP)
Published: March 19, 2025
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Guide to Post-Market Clinical Follow-up Requirements Under EU MDR (2017/745)
Published: March 18, 2025
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Understanding the New FDA Draft Guidance on Medical Device Chemical Characterization
Published: March 14, 2025
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