SOGQS MEDICAL DEVICE CONSULTANCY Kundli Sonipat

TRANINIG AND CONSULTENCY 1.ISO 13485:2016 2.MDD 93/42 EEC 3.EUROPEAN MDR 2017/745 4.CE MARKING FOR MEDICAL DEVICES 5.ISO 14971:2012-RISK ANALYSIS 6.93/42/EEC-Medical Device Directive 7.EU MDR 2017/745-Medical Device Rule 2017 8.Indian MDR 2017-Indian Drug and cosmetic act 1940 9.USFDA 21 CFR 820-QMS for USA 10. MANUFACTURING LICENSE, BRAND APPROVAL, LOAN LICENSE,WHOLESALE LICENSE, CLEAN ROOM APPROVAL 11.FREE SALE CERTIFICATE, MARKET STANDING CERTIFICATE, QUALITY AND CAPCITY CERTIFICATE, NON CONVECTION CERTIFICATE