
“The quality and coverage of B2B contact database are very impressive...”
Mark J.
`
+15
inmedis is your Swiss partner for quality management and regulatory affairs in the medical device industry. Our experienced experts support you pragmatically and goal oriented in the following areas: - Quality management systems: ISO 9001 / ISO 13485 / FDA QSR / Audits / MDSAP - Interim Quality Management Resources: Outsourcing of QM/RA functions / coaching and support - Technical Documentation: MDR-compliant technical documentation / gap analyzes / reviews - Validation: Design and manufacturing processes / Computer systems (CSV) - Biocompatibility: Planning and implementation / ISO 10993 - Regulatory affairs: Approval strategy and registrations / Post-market surveillance and standards monitoring...
Iso 13485,fda qsr,audits,mdsap,risikomanagement,iso 14971,mdr,mepv,prrc,technische dokumentation,designvalidierung,prozessvalidierung,computersystemvalidierung (csv),sterile verpackungssysteme,biokompatibilität,iso 10993,produktzulassungen,marktüberwachung (pms),vigilanz,and normenüberwachung
Inmedis gmbh operates in the Medical equipment manufacturing industry.
Inmedis gmbh's revenue is 11m - 100m
Inmedis gmbh has 11 - 50 employees.
Get Started with the Free Forever plan! No credit card needed. Enjoy up to 10,000 free email credits per month at no cost.
Start Prospecting from Clodura.AI's database of 600M+ verified B2B contacts and 120M+ direct dials along with 18M+ companies' org charts.
Unlock the prospect's contact details, including verified email, direct dials, add them to cadence, and close more deals.