Market Access & Post-Market

Complife
Market Access & Post-Market
Acerca del proveedor
Via Giuseppe Saragat 5
40026 Imola
Italy
Certificaciones
  • ISO/IEC 17025 ISO/IEC 17025
  • ISO 13485 ISO 13485
  • ISO 9001 ISO 9001
Descripción

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

Cada hora
0,00 €
Diario
0,00 €
Semanal
0,00 €
Mensual
0,00 €
Tarifa plana
0,00 €
Mercado
  • Europa
  • Asia
  • África
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