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QES Medical strengthen position. Signs collaboration agreement w/ European Software Development Firm

NOV. 23, 2021. QES Medical LLC signs a collaboration agreement with European Medical Software Development Firm Atostek, which is a leader in the industry and is expanding its presence in the United States. This collaboration agreement is strengthening QES Medical LLC’s position to help clients achieve faster time to market for their medical devices, always ensuring compliance with the applicable regulatory requirements.


QES Medical LLC is a consulting firm, founded in 2009, providing a variety of quality and regulatory services to the medical device industry. We help medical device companies achieve and maintain QMS certification and cGMP, as well as product regulatory clearance. Visit our website www.qesmedical.com to learn more about us!


About Atostek: “Atostek offers services for the software development of medical devices. We have been awarded the ISO 13485 certificate for medical devices and software, which applies to development of medical software for clients. We also guarantee that we operate in accordance with the applicable regulatory requirements.” Visit https://atostek.com/en/services/software-development-for-medical-devices/ to learn more.

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Responsibilities Actively execute quality assurance in design development, including but not limited to: Support design control deliverables. Author verification and validation protocols and reports.