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GENERAL · life-sciences

Conduct GxP Audit

Conduct a GxP audit of computerized systems and processes. Covers audit planning, opening meetings, evidence collection, finding classification (crit…

pjt222
GENERAL · life-sciences

行 GxP 稽核

Conduct a GxP audit of computerized systems and processes. Covers audit planning, opening meetings, evidence collection, finding classification (crit…

pjt222
GENERAL · life-sciences

Conduct GxP Audit

Conduct a GxP audit of computerized systems and processes. Covers audit planning, opening meetings, evidence collection, finding classification (crit…

pjt222
European Union flagEuropean Union · life-sciences

Senior MDR 2017/745 Specialist and Consultant

EU MDR 2017/745 regulation specialist and consultant for medical device requirement management. Provides comprehensive MDR compliance expertise, gap …

ovachiever
European Union flagEuropean Union · life-sciences

MDR 2017/745 Specialist

EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Co…

borghei
CROSS-JURISDICTION · life-sciences

KSB-D07-K0033: Policy Interpretation

Policy Interpretation: Guidance document analysis, regulatory precedent evaluation, interpretation consistency, implementat...

nexvigilant