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Mantra Systems Ltd

An effective Post-Market Clinical Follow-up (PMCF) system is an essential component of all regulatory frameworks under the MDR & our in-house team of medical professionals have the clinical experience and extensive knowledge of the study design techniques required for successful regulation of your medical devices. We will produce a GDPR-compliant data collection system designed around the bespoke needs of your product, enabling investigators and patients to securely input data directly into the PMCF study. Our PMCF service offers:- Professional PMCF study design Detailed knowledge of medical device registry and survey design techniques. Real-time data collection & storage Curated eCRF, ePRO and data storage systems enabling secure data collection from any device Technical document writing PMCF Plans, Protocols, Investigator's Brochures, ICFs and PMCF Reports written by medical experts Start by contacting us for a free consultation and quote to discuss your PMCF requirements.


medical device

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