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Services

Clinical Project Coordination

From first concept to market release, the regulatory path for medical devices is demanding — and the details matter. Kamelion supports you throughout the clinical development process, keeping your project structured, your documentation complete, and your timelines realistic.

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  • Study design tailored to your device class, risk classification, and intended use

  • Full document compilation, including clinical evaluation reports and post-market follow-up plans

  • Ethics committee and IRB proposals, prepared and submitted worldwide

  • Ongoing communication and correspondence with regulatory authorities

  • Clinical investigations designed and conducted in accordance with MDR and ISO 14155

  • US market entry support: FDA 510(k), Investigational Device Exemption (IDE), and Q-Submission

Medical Affairs & Medical Science Liaison (MSL)

Bringing a product to market requires more than strong data — it requires the ability to communicate that data clearly, credibly, and strategically. Kamelion provides Medical Science Liaison expertise on a flexible basis, helping you establish scientific positioning and engage the right stakeholders at the right time.

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  • Expert communication of clinical and scientific evidence to internal and external audiences

  • Assessment of state-of-the-art treatment options and competitive landscape

  • Support for medical affairs strategy and stakeholder mapping

  • Liaison between R&D, regulatory, and commercial teams

  • Available project-based or as interim MSL support for a defined period

Medical Writing & Editing

Good science deserves clear writing. Kamelion provides professional medical writing and editing services following GPP3 guidelines, ensuring your documents are accurate, compliant, and ready for submission or publication — the first time.

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  • Study protocols and amendments

  • Clinical study reports and other study documents

  • Ethics committee and IRB proposals

  • Grant proposals and funding applications

  • Manuscripts, including revision support and response to reviewers

  • Abstracts for conferences and publications

  • Plain language summaries and texts for general audiences

  • Presentations for healthcare professionals and scientific meetings

Customized Webinars and Workshops

Your product is only as strong as the team behind it. Kamelion designs and delivers customized webinars and workshops that help your colleagues understand the clinical, regulatory, and strategic context of their work — so everyone pulls in the same direction.

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  • Tailored content for your specific audience: engineers, executives, sales, or cross-functional teams

  • Topics include clinical implications of device design, regulatory landscape overview, R&D strategy & prioritization, and more

  • Interactive format: questions, case discussions, real-world examples

  • Available as half-day workshops, full-day intensives, or focused 60-minute webinars

  • Remote or on-site delivery

How may we help you?

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