Menu
Design & Engineering
Medical Device Development
Mechanical Design
Pre-series and Prototype
Usability & HFE
Finite Element Analysis
Composite and Biopolymers
Injection Molding
PEEK and Carbon Fiber Implants
Reverse Engineering – Laser Scanning
3D Tomography Analysis
Rapid Prototyping
Quality & Validation
MDSAP – Medical Device Single Audit Program
Quality System Support
ISO 13485 Auditing Service
SOP – IOP
VMP IQ/OQ/PQ Validation
Clean Room Design and Validation
Regulatory Support
MDR 2017/745
European Authorized Representative Service
CH-REP – SAR Swiss Authorized Representative service
EU PRRC
Technical File Design Dossier
Clinical Evaluation
DHF Design History File
Risk Management Process
ISO 14971:2012 – 2019 Gap Analysis
Design Control Process
Testing
Mechanical Test Fatigue Static
Biological Safety Evaluation
ISO 10993-17 Toxicological Evaluation
Cardiovascular Digital Simulation Model
Electronic IFU (e-IFU)
No products in the cart.
Home
Shop
Shop
Showing the single result
Default sorting
Sort by popularity
Sort by average rating
Sort by latest
Sort by price: low to high
Sort by price: high to low
MDR Classification Document
CHF
200.00
Add to cart
Back to Top