Izdelki za prc oblika zdravila (2)

Tehnična Dokumentacija MDR

Tehnična Dokumentacija MDR

Our experienced team has for years done documentation for companies who are manufacturers of medical devices /surgical instruments. We provide Quality-Management-Systems for meeting legal and normative requirements. For manufacturers of medical devices / surgical instruments class I (including Is, Im, and new for MDR class Ir), IIa, and IIb we offer the following services:
 Implementation DIN EN ISO 13485 and the EU-Regulation 2017/745 MDR and 21 CFR 820 QSR Creating QM-Systems with procedural instructions and work instructions Technical Documentation Clinical evaluation Risk Management / Risk Analysis Essential Safety and Performance Requirements Validation of processes UDI-labeling Consulting for Regulatory Affairs Internal audits and external supplier audits Accompaniment and support with inspections by authorities and Audits by notified bodies Communication with authorities
1-Metoksi PMS - Fine Kemikalije

1-Metoksi PMS - Fine Kemikalije

Product group: Reagents CAS-Nr.: [65162-13-2] GHS pictogram: GHS07GHS08 Shipping condition: ambient MW: 336.36g/mol Formula: C15H16N2O5S CAS Nr:[65162-13-2] Code:M003 Manufacturers:Dojindo