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Device Love by R&Q

Device Love by R&Q

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RQM+ industry-leading experts and often special guests discuss regulatory, quality, clinical, lab, and reimbursement challenges MedTech companies are facing. RQM+ is the world’s leading MedTech service provider offering consulting, clinical trial, lab, and reimbursement services, as well as technology solutions to support the entire product lifecycle. With more former FDA, Medicines, and Healthcare Products Regulatory Agency (MHRA) and notified body regulators than any other firm, the RQM+ team has deep expertise in all clinical specialties. Please visit RQMplus.com to learn more.

Recent Episodes

  • Carrie Schneider, Principal Consultant | Excellence Spotlight

    1 week ago

  • What makes a successful regulatory submission from a clinical trial perspective for IVDs? – MedTech CRO: Regulatory Expertise Series

    2 weeks ago

  • Holly Cotter, Senior Consultant | Excellence Spotlight

    3 weeks ago

  • What makes a successful regulatory submission from a clinical trial perspective? (Part 3/3) – MedTech CRO: Regulatory Expertise Series

    4 weeks ago

  • Live! #83 – Structured Dialogue: How to Engage with Notified Bodies

    4 weeks ago

  • What makes a successful regulatory submission from a clinical trial perspective? (Part 2/3) – MedTech CRO: Regulatory Expertise Series

    1 month ago

  • Christine Anderson, Principal Consultant | Excellence Spotlight

    1 month ago

  • What makes a successful regulatory submission from a clinical trial perspective? (Part 1/3) – MedTech CRO: Regulatory Expertise Series

    1 month ago

  • Michael Louis, Chemist II (Jordi Labs) | Excellence Spotlight

    1 month ago

  • Best Practices In AE Reporting In Clinical Trials – MedTech CRO: Clinical Trial Execution Series

    1 month ago