Medidee Services SA is a leading end-to-end consulting service provider for the MedTech industry, now part of Veranex. They offer comprehensive regulatory, clinical, and quality management solutions.
Medidee Services SA, now part of Veranex, is a premier end-to-end consulting service provider dedicated to the MedTech industry. They specialize in guiding companies through all product development stages, from initial concept to regulatory clearance and certification. Their expertise spans critical areas including Regulatory Affairs (CE-Marking, MDR/IVDR transition, US FDA submissions), Clinical Affairs (CRO services, clinical strategy, trial execution), and Quality Management Systems (ISO 13485, MDSAP). Medidee also provides specialized services such as EC Representative functions for non-EU manufacturers and GDPR data protection consulting. With a focus on integrating patient safety and business objectives, Medidee helps clients navigate complex regulatory landscapes, select appropriate pathways, and manage interactions with authorities and notified bodies. They offer tailored solutions for a wide range of medical devices, including In Vitro Diagnostics, Digital Health, Combination Products, and Implantables.
About
**Who they are** Medidee Services SA is a consulting service provider for the MedTech industry, now part of Veranex. They are based in Switzerland and offer comprehensive regulatory, clinical, and quality management solutions.
**Expertise & scope** * End-to-end consulting for the MedTech sector * Regulatory, clinical, and quality management solutions * Services tailored for the Swiss market
**Reputation / proof points** * Part of Veranex
Additional information
Medidee Services SA focuses on providing comprehensive support for MedTech companies navigating complex regulatory landscapes. Their services are designed to ensure compliance with Swiss requirements, offering a local presence and expertise. Buyers can expect a structured approach to regulatory, clinical, and quality management, facilitating market access and ongoing compliance for medical devices. Engagement typically involves detailed project scoping to address specific client needs within the MedTech industry.
Key Highlights
Part of Veranex, a global product development and commercialization partner.
Source
“Medidee Services SA is a leading end-to-end consulting service provider for the MedTech industry, now part of Veranex.”
Offers comprehensive regulatory, clinical, and quality management solutions.
Source
“They offer comprehensive regulatory, clinical, and quality management solutions.”
Companies requiring end-to-end regulatory, clinical, and quality management support
How engagement typically works
Consultative approach
Project-based engagements
Typical deliverables
Regulatory strategy and submissions
Clinical trial support
Quality management system implementation
Swiss Authorized Representative services
Good to know
Best when requiring specialized MedTech regulatory expertise for the Swiss market
HQ: Lausanne, CH
Languages: English, German, French
Timezones: Europe/Zurich
Claim status: Listed
Services & Capabilities
Best CH-REP (Swiss Authorized Rep) | Compare & Get Quotes
Jurisdictions: CH
Countries: CH
Industries: Medical devices, IVD
Portfolio: 6-25, 26-100
Onboarding time: 3–10 days
Pricing model: Onboarding + annual retainer
Starting from: CHF 2,400
Included services: Swissmedic contact point handling, Vigilance and incident reporting coordination, Labeling/packaging CH-REP information alignment, Mandate administration and documentation availability, Quality management consulting