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مراجع و فرم ها

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IEC 62304

Medical device software Software life cycle processes

IEC 62366

Medical devices – Part 1: Application of usability engineering to medical devices

INSO 3001-1

سترونی وسايل پزشکی-آزمون سترونی قسمت1روش مستقیم

INSO 3001-2

سترونی وسايل پزشکی-آزمون سترونی قسمت :2روش صافی غشايی

INSO 18024

ارزيابی ضدعفونی کننده های اتاق تمیز- آيین کار

ISO 10993-1

Biological evaluation of medical devices Part 1: Evaluation

ISO 10993-5

Biological evaluation of medical devices Part 5 Tests for in vitro cytotoxicity

ISO10993-10

Biological evaluation of medical devices Part 10: Tests for skin sensitization

ISO 13485-2016

Medical devices — Quality management systems

ISO 14971-2019

Medical devices — Application of risk management to medical devices

ISO-TR-24971

Medical devices — Guidance on the application of ISO 14971

MDR 2017-745

REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL

ISO 15223

Medical devices Symbols to be used with information to be supplied by the manufacturer Part 1: General requirements

MDR-3_441

دستورالعمل گزارش مشکلات کیفی، حوادث ناگوار و بازفراخوانی تجهیزات پزشکی