The world’s most popular standard for medical device quality management has revised in 2016 by ISO. Global Certification Consultancy introduces QMS Medical Devices documentation for manufactures industries with reference of requirements of ISO 13485:2016 standard. Our medical devices documents are created by team of internal auditors and consultants with highly expertise in implementing QMS system for many global clients. The company announced to start selling it on website www.certificationconsultancy.com
The medical devices certification documents will be very helpful tool for creating documents for ISO 13485:2016 certification as well as to upgrade and to implement quality management system in medical devices manufacturing company. The product is readymade ISO 13485:2016 documents that will be delivered to buyer in .doc files (soft copy), which are easily editable. Such medical devices manufactures documents contain quality manual, mandatory procedures, SOPs, sample formats as well as clause wise and requirements wise audit checklists, which will help to create transparency and compliance with fair triaging legislation in Medical Devices documentation.
The Medical Devices Documentation Kit, which is available with free sample DEMO in .pdf format, can be purchased online at just 399 USD via secure transaction through paypal.com. Clients around the world have already used it and committed that they have completed documentation process in less time. The total documentation kit for ISO 13485 can be a good tool to use as reference or directly used with editing as it is designed in .doc format in simple English. For any organization going for upgrading their existing system or first time implementing Quality management system for ISO 13485:2016 certification, these documents can be easiest guide to understand implementation and documentation process as per updated standard for quality management systems in medical devices manufacturing organizations.