From Complexity To Clarity: Decoding Medical Device Regulatory Intelligence And Medical Device Regulatory Compliance

Whether it is high or low risk, digital or physical devices, pure-play or combination medical devices – regulatory authorities have strict regulations for all to ensure its safety and efficacy. This demands for careful attention by the medical device manufacturers to the medical device regulatory requirements, medical device regulatory information, medical device registration, safety evaluations and QMS. To decode the regulations and device a suitable medical device regulatory strategy, Freyr offers the best of both worlds – a fully configurable software solution with a suite of regulatory intelligence solutions and services that offers best in class, cost-effective and customizable solutions built around your unique requirements covering medical device regulatory compliance across your medical device lifecycle.

We provide intelligence that helps you with medical device classifications, labelling, registrations, approvals, and post-market surveillance. You get access to 5000+ insights categorized into risk classes & product types. With an extensive coverage of global medical device regulations across drug-device combinations, in-vitro diagnostics, digital health products and more, we help startups and developed companies achieve medical device regulatory compliance by medical device regulatory information updates hence, navigate the ever-changing world complex regulatory landscape.

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Discover Medical Devices Intelligence
Annual Reports Post-Approval Changes License Renewal/Transfer Post-Market Surveillance, Complaints, and Adverse Events, Product Improvements, External Body Audits, New Market Launches and Materiovigilance Import/Export and In-country Specific Requirements Labeling (including IFU) and Packaging Advertising and Promotion Labeling (including IFU) and Packaging QMS and Compliance Facility Audits, Site Registration Requirements Technical Documentation, General Procedures, Timelines and Fees Submissions - Certificates, Risk Classification, Samples, Language, Testing Real World Data and Real World Evidence Regulatory Strategy Clinical Trials, Risk Analysis
Periodic regulatory updates that are customised per your products and markets of interest Fully configurable workflows that can be customised for steps, stakeholders, timelines and sequence. Innovative chatbot empowered with ChatGPT technology and Freyr's proprietary training dataset. Powerful search capabilities (filters that work in combination for topic, product type, market, and a range of dates) Difficult to catch up with regulatory changes that impact my Product Portfolio We want not just a database or platform for individual consumption, but we also want to collaborate with our colleagues and partners (assigning task, collating impact assessment, tracking the implementation) Difficult to find the relevant regulations and clear, concise answers instead of just a stack that has thousands of documents

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