GOST R 57502-2017 PDF

GOST R 57502-2017 Referenced Document

GOST 2.101-2016 Unified system for design documentation. Types of products
GOST 2.102-2013 Unified system for design documentation. Types and sets of design documentation
GOST ISO 13485-2011 Medical devices. Quality management systems. System requirements for regulatory purposes
GOST ISO 14971-2011 Medical devices. Application of risk management to medical devices
GOST R 12.1.019-2009 Occupational safety standards system. Electrical safety. General requirements and nomenclature of kinds of protection
GOST R 12.3.047-2012 Occupational safety standards system. Fire safety of technological processes. General requirements. Methods of control
GOST R 50444-1992 Medical instruments, apparatus and equipment. General specifications
GOST R 51897-2011 Risk management. Terms and definition
GOST R 51898-2002 Safety aspects. Guidelines for their inclusion in standards
GOST R 7.0.8-2013 System of standards on information, librarianship and publishing. Records management and organization of archives. Terms and difinitions
GOST R IEC 60601-1-2010 Medical electrical equipment. Part 1. General requirements for basic safety and essential performance
GOST R ISO 14041-2000 Environmental management. Life cycle assessment. Goal and scope definition and inventory analysis