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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Featured Capabilities:

Document Management Product Development Design Control Risk Solutions Training Management CAPA Management

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys

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Learn valuable, career-boosting skills for the Medical Device industry. Get access to hundreds of free resources as well as subscription-based courses and certifications.

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Ultimate Guide to ISO 14155:2020 for
Medical Devices

The ultimate guide about ISO 14155:2020 and Good Clinical Practices (GCP) packed with valuable insights into how to conduct and plan a clinical investigation in compliance with ISO 14155:2020.

       Ultimate Guide to ISO 14155 (cover)-1

 

 

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