Qarad offers the following services:

Training, consulting and coaching with respect to:

• In Vitro Diagnostics Directive 98/79/EC and Medical Device Directive 93/42/EC
• Quality system requirements
• Technical Documentation, Design Dossiers
• Risk Analysis
• Labeling, Translations
• Notified Body approval and Conformity Assessment Procedures
• ISO9001, ISO13485 and ISO17025 certification. FDA QSR compliance.
• European Directives on dangerous substances and preparations (Material Safety Data Sheets, Labeling)

Organization and monitoring of performance evaluations

Quality system audits of suppliers or in the context of Due Diligence

Authorized Representative in the context of European new approach directives

Contact Information

Qarad
Volmolenheide 13
B-2400 Mol
Belgium