info@1med.ch

Your Global Full-Service CRO Partner for MedTech, Pharma & Biotech

We are a leading international solutions provider, offering comprehensive end-to-end expertise in MedTech, pharmaceutical drug development, novel technologies, and combination products.

Expert support in MedTech, Pharma & Biotech

At 1MED, we are dedicated to continuous growth and excellence.

We provide specialized support to the MedTech, Pharmaceutical and Biotech industries, partnering with our clients to guide them through every phase of development.

Our commitment to innovation drives us to constantly evolve and strengthen our capabilities. By embracing new technologies and methodologies, we offer comprehensive, cutting-edge solutions designed to meet the unique challenges of our clients. This dedication ensures we remain a reliable and trusted partner, committed to helping you bring transformative products to market.

Solutions

We are committed to ensuring the success of your projects by providing holistic guidance on product development, starting with the implementation of Quality Management Systems meeting ISO 13485 standards, regulatory consultancy for Technical Documentation and Clinical Evaluations compliant with MDR and IVDR, and comprehensive support for clinical studies across all phases in Europe and beyond.

Quality
Services

We offer customized regulatory and quality solutions designed for medical device companies.

Clinical Services for MedTech

We provide end-to-end support covering each step of a clinical investigation, from First In Human (FIH) to observational registries.

Clinical Services for Biotech & Pharma

We support companies through every stage of clinical development, offering tailored solutions that streamline regulatory pathways and accelerate the launch of safe, effective therapeutics.

Regulatory Services

We offer customized regulatory and quality solutions designed for medical device companies.

Post-Market Services

Providing a comprehensive post-market support to ensure regulatory compliance and enhance the safety and performance of your medical device throughout its lifecycle.

Why us

We tackle your challenges as our own, accelerating the regulatory and commercial processes of your medical devices, combination products, and in vitro diagnostics. As an ISO 13485 certified company, we blend reliability with the agility of a start-up, offering regulatory support, digital solutions, and full-service CRO assistance.

Our lean, transparent approach ensures clear insights into risks, benefits, costs, and timelines. With global expertise and a dedicated MedTech focus, we advance your projects from innovation to commercialization, improving patient health and well-being. Together, we are dedicated to realizing your vision, and united, we will achieve extraordinary success.

Insights

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