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Lacidem develops and implements clinical and medical programs for medical device and pharmaceutical companies with a specific focus on the European markets.

New legal (MDR/ IVDR) requirements for medical devices are reinforcing the need for compelling clinical arguments based on performance and safety, efficacy and risk/benefit ratios. Lacidem has the knowledge, experience and skills to support medical device companies lacking the resources to perform this work.

For pharmaceutical companies, Lacidem can act as and external medical affairs department in situations with no or limited medical resources.

Develop clinically relevant products

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Our activities can be divided in 5 categories 

  • Clinical evaluations
  • Medical affairs
  • Clinical research
  • Clinical marketing
  • Post-market surveillance (PMS), post-market clinical follow-up (PMCF) and vigilance support

Lacidem
Wilhelminalaan 6
3761 DN Soest

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