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Official documents
This section contains all the updated regulations and documents that regulate the activity and services of ECM. You can consult them by clicking on the reference category and selecting the document you want to view.
REGULATIONS
- Regolamento Certificazione Volontaria Non Notificata (RGVOL01)
- Note of the EU Commission on Voluntary Certification REF. ARES (2022) 6342894
- RGPRD_Product Certification Regulation
- RGPRD-A2_Machinery Directive 2006/42/EC
- RGPRD-A3_Direttiva Rumore 2000/14/CE
- RGPRD-A4_EMC Directive 2014/30/EC
- RGPRD-A5_PED Directive 2014/68/EU
- RGPRD-A6_ATEX Directive 2014/34/EU
- RGPRD-A7_RED Directive 2014/53/UE
- RGPRD-A8_Lifts Directive 2014/33/EC
- RGPRD-A9_Regulation PPE 2016/425/EU
- RGPRD-A10_Regulation UAS 2019/945/EU
- Regulations for Medical Device Certification (MDR)
- Regulation of Legacy Medical Devices (MDD)
- SG_14 Regulation for the Quality Management Systems Certification
- RTVPS_Regulation of Periodic and Extraordinary Verifications
- RTVP 81-2008 Regulation of Periodic Verification D. Lgs. 81/2008
ACCREDITATION CERTIFICATES AND OTHER ATHORIZATIONS
- Accreditation Certificate for ISO / IEC 17065 Product Certification
- Authorization to issue CE Certification of Medical Devices
- Authorization Decree Directive 2014/33 / EU – Lifts
- Authorization Decree Directive 2006/42 / EC – Machinery
- Authorization Decree Directive 2014/34 / EU – Atex
- Authorization Decree Directive 2000/14 / EC – Noise
- Authorization Decree Directive 2014/30 / EU – EMC
- Authorization Decree Directive 2014/68 / EU – PED
- Authorization Decree Directive 2014/53 / EU – RED
- Certificate of Accreditation ISO / IEC 17021 Quality Management Systems
- ISO / IEC 17025 Testing Laboratory Accreditation Certificate
- Certificate of Accreditation ISO / IEC 17020 Inspection Body
- Certificate of Qualification as National Certification Body (NCB)
- Authorisation Decree 81/2008 – periodic verifications
APPLICATION FORMS, QUOTATIONS AND INFORMATION REQUEST
- Communication of changes to legacy devices
- Medical Device Certification Application – MDR 2017/745
- ECM price list of conformity activities under MDR
- QMS Certification Application
- Request Form for Periodic Verification Groups SC (Things Lifting) and SP (People Lifting)
- Request Form for Periodic Verification of GVR Group (Gas, Steam, Heating)
- Request Form for Quotation D.P.R. 462/2001
