About the Supplier
Via Giuseppe Saragat 5
40026 Imola
Italy
Certifications
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ISO/IEC 17025
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ISO 13485
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ISO 9001
Description
Industrial gap/problem covered
Successfully launching and maintaining a medical device in the market requires a solid regulatory strategy, proper documentation, and continuous post-market monitoring. Many companies struggle with navigating complex regulatory pathways, ensuring proper registrations, and complying with evolving post-market surveillance requirements. Failure to meet these demands can lead to delays in market entry, regulatory penalties, or even product withdrawal.
Description
We formulate a regulatory strategy to allow the entry of the medical device in the target market and we support our client in all the necessary actions to maintain its presence over time.
- Product documentation
- Registrations
- Local Representative
- Post-Market Surveillance
Hourly
€0.00
Daily
€0.00
Weekly
€0.00
Monthly
€0.00
Flat Rate
€0.00
Market
- Europe
- Asia
- Africa