Medical Technology Regulations | ARTED Rules and Standards

ARTED

Guideline on Clinical Trial Applications to TITCK Clinical Trials Department
Free Promotional Sample Distribution and Press Release Application Guide
Guide to Audits and Assessments by Notified Bodies in the Field of Medical Devices
Guideline on the Registration of the Product Tracking System of Medical Devices
Guideline on Phase 1 Clinical Trial Centers
Guideline on the Import of Investigational Products to be Used in Clinical Trials
Guideline on Trainings Organized within the Scope of the Regulation on Testing, Control and Calibration of Medical Devices
Guideline on the Implementation of the Provisions of Circular No. 2020/6 on the Registration of Medical Device Technical Service Providers and Related Technical Personnel
Guideline on Product Tracking System Single Motion Notifications of Medical Devices
TCOKKA - Guidelines on the Implementation of Article 59 of the Medical Device Regulation and Article 56 of the In Vitro Diagnostic Medical Device Regulation
Guideline on Scientific Meetings and Educational Activities to be Held within the Scope of Medical Device Sales, Advertising and Promotion Regulation
Guideline on the Implementation of the Provisions of the Regulation on Quality Compliance and Quality Control Tests of Diagnostic Radiology, Nuclear Medicine and Radiotherapy Group Medical Devices
Guideline on Scientific Meetings and Educational Activities to be Held within the Scope of Medical Device Sales, Advertising and Promotion Regulation
Guideline on Testing,Controlling and Calibration Activities to be Conducted within the Scope of the Regulation on Testing, Controlling and Calibrating Medical Devices (Version No 3)
Guideline on the Implementation of the Provisions of the Regulation on Technical Services of Medical Devices Used within the Scope of Health Service Delivery
Guideline on the Implementation of the Medical Device Sales, Advertising and Promotion Regulation

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