Regulatory consulting service supporting medical device manufacturers through MDR (Medical Device Regulation) compliance, including design control, risk management, quality management system development, and international market authorization documentation.
Manufactured by
TS Quality & Engineering SRL
Cantarana, Italy
TS Quality Engineering is a ISO 13485 certified company. We offer Medical Device Consulting Services and solutions aimed at facilitating, speeding up and support design, validation, regulatory processes and streamline worldwide market acces.
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Freudenberg Medical Europe GmbH
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STATICE SAS
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3 of 112 closest product alternatives
Freudenberg Medical Europe GmbH · Germany
Regulatory guidance and support services for medical device development and commercialization. Services assist customers in meeting quality standards and regulatory requirements globally.
Murrplastik Medizintechnik GmbH · Germany
Regulatory approval and certification assistance for medical devices manufactured in-house, including compliance guidance and quality assurance documentation.
STATICE SAS · France
Regulatory support and homologation services for medical devices across multiple international markets, ensuring compliance for Class I-III devices.
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