CleanControlling
Technical
Medical
Chemical
Materials
de
en
Services
Biological analytics
Cleaning of medical devices
Reprocessing of medical devices
Sterilization of reusable products
End-of-life simulation reprocessing cycles
Hygiene / Hospital Hygiene
Chemical analytics
Chemical characterization - DIN EN ISO 10993-18
Toxicological evaluation - DIN EN ISO 10993-17
Unknown substances
Particle analytics
Particle contamination of medical devices
Material identification of particles
Analytics of AM products
Events
Infothek
Testing methods
Bioburden Determination
In vitro cytotoxicity test
Endotoxin test
TOC Determination
THC Determination
Norms and Standards
Bioburden
Cytotoxicity, biocompatibility
Endotoxin test (LAL test)
TOC determination of water-soluble organic contaminants
Particles in medical technology
Accreditation
Order processing
Contact
Contact form
Direct contacts
Driving Directions
CleanControlling
Technical
Medical
Chemical
Materials
Search form
Standards on particles in medical technology
VDI 2083 Part 21 Cleanliness of medical devices in the manufacturing process
USP 36 <788> Particulate matter in injections
ASTM F2459 Standard Test Method for Extracting Residue from Metallic Medical Components and Quantifying via Gravimetric Analysis
ISO 16232:2018 / VDA 19.1 Road vehicles - Cleanliness of components and systems
Newsletter registration
You find more information about our medical newsletter here!
Submit
www.CleverReach.de
2024 © CleanControlling GmbH
Sitemap
Download
Privacy Policy
Terms & conditions
TISAX
Imprint