Medical Device Testing
Smithers Medical Device Testing helps medical device and pharmaceutical product manufacturers bring innovative, compliant and highly effective products to market with our world-class expertise and extensive independent medical device testing capabilities.
We can assist throughout your medical device product development cycle, with medical device testing from concept, material selection, design for manufacture, manufacture, packaging (primary and secondary) through to the distribution testing for supply chain validation.
Our experienced team will provide advice, guidance and recommendations as well as delivering test data to help you demonstrate compliance to regulatory guidance or specifications set out by the FDA, EMA, MHRA, USP, ASTM and ISO.
Our global conferences and market reports provide an independent and expert view of emerging markets, technologies and disruptive factors. We also offer bespoke consultancy services, helping companies solve specific business issues and assisting with strategic business planning.
Physical and Functional Testing of Medical Drug Delivery Devices
Physical and Functional Testing of Medical Drug Delivery Devices
Smithers Medical Device Testing provides standard and non-standard medical device testing (ISO, ASTM or Pharmacopeia) on a wide range of drug delivery devices, accessories and packaging to ensure products are compliant and fit for use.
Healthcare Packaging Testing
Healthcare Packaging Testing
Smithers provides a range of packaging services to ensure that medical products are packed in such a way that their characteristics and performance during intended use will not be adversely affected during transport and storage.
Medical Device Technical Consulting
Medical Device Technical Consulting
Smithers Medical Device Testing world-class technical team will help you solve problems and optimise your materials, device and packaging.
Medical Device Regulation (MDR)
Medical Device Regulation (MDR)
Smithers Medical Device Testing provides comprehensive services to the pharmaceutical, biopharmaceutical and medical device industries in support of the new Medical Device Regulations (MDR).