Management of documents is complicated where an accurate eQMS solution will help companies in creating automation and efficiency greatly. Document management is a vital component in ascertaining the quality of the medical device with ISO 13485. The Quality Mangement System (QMS) capabilities should have the incorporation of the links to all methods which can impact product quality, compliance, and safety.
We at GQS helps clients in identifying the robust skills for document archival along with the smart search easy document retrieval. It should also note that the regulatory risk isn’t a component to consider much about and ineffective ISO 13485 documents can facilitate issues with great product assurance. GQS Singapore provides efficient document draft collaboration with an automated document routing for approval in countries like; Singapore, Malaysia, Philippines, Indonesia, Myanmar, Vietnam, Korea, Cambodia, etc. If you want any help related to the 13485 Medical Devices’ certification, you can drop an email to [email protected].
