ISO 9001:2015
It is a globally accepted and highly compatible standard that assures
ISO Stands for International Standards of Organization. ISO is an independent, non-governmental international organization with a membership of 162 national standard bodies.
Certification can be a useful tool to add credibility, by demonstrating that your product or service meets the expectations of your customers. For some industries, certification is a legal or contractual requirement.
ISO 13485, compliance with requirements includes compliance with regulatory requirements. Thus, for devices used in the United States to comply with ISO 13485, manufacturers must also comply with the QS Reg. standard. As a regulation, QS Reg. Is often more specific than ISO 13485, particularly in the areas of claims handling, labeling control and documentation. ISO 13485 is structured similarly to ISO 9001: 2000 and is actually 90% the same as the general standard for quality management systems..
What is ISO 13485?
ISO 13485 Medical Device - Quality Management System - Requirements for regulatory purposes is a standard of the International Organization for Standardization (ISO) first published in 1996; It represents the requirements of a complete quality management system for the design and manufacture of medical products.
Fast & Hazel Free Process, Best service at Best Price Guaranteed, Certificate Valid Internationally, Tender and Assistance on ISO Certification.
ISO Stands for ISO Global Certification. ISO is an independent, non-governmental international organization with a membership of 162 national standard bodies.
+91-7400016631 Enquiry Now
Commit to working consistently without pause
Cost-effectiveness analysis is a form of money
Significant of teamwork: Fresh ideas. Learning new skills
I prioritize my work around clients. I will be there
Customer-First On-Time Delivery Commitment. Working Project
If you want to talk Anytime Anywhere Anyplace
Have any queries? Get in touch freely.
