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Corporate
About Us
Logos
Management’s Commitment
Quality Policy
Accreditations
Our Services
System Certification
EN ISO 13485:2016
Trainings
Standart Trainings
EN ISO 14971:2019 Product Risk Management
ISO 13485:2016 Medical Device Quality Management System
Regulational Trainings
MDR:2017/745
Special Process Trainings
Validation Trainings
Documents
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English
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TL.05 Quality Management System Customer Information Instruction
TL.05 Quality Management System Customer Information Instruction
PR.03 Objection, Complaint and Dispute Evaluation Procedure
PR.03 Objection, Complaint and Dispute Evaluation Procedure
PR.06 Certificate and Brand Usage Procedure
PR.06 Certificate and Brand Usage Procedure
TL.02 Remuneration Instruction
TL.02 Remuneration Instruction
FR.08 Objection and Complaint Process Evaluation Questionnaire
FR.08 Objection and Complaint Process Evaluation Questionnaire
FR.20 Management System Application Form
FR.20 Management System Application Form
FR.21 Amendment Notification Form
FR.21 Amendment Notification Form
REGULATION (EU) 2017/745 OF THE EUROPEAN
REGULATION (EU) 2017/745 OF THE EUROPEAN
