Formulation of Innovative Projects

Rational Medical

Writing Medical-Scientific Reports to support and endorse products on the market aimed at Regulatory Entities, Doctors, and much more.

Writing of Medical-Scientific Reports to support and endorse products on sale aimed at:

  • Regulatory Entities.
  • Doctors.
  • Marketing Literature.
  • Patients.
  • Treatment Communities.

A search and identification of international bibliography is carried out, its analysis and document writing.

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Clinical Studies - Phase I Trials

We conduct Phase I to IV Clinical Research studies with the highest quality standards. A team made up of Medical Specialists from our research units together with the team of Medical Researchers form a group in charge of developing the protocols.

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Bioavailability-Bioequivalence Studies

We are leaders of design, execution, and analysis of Bioavailability-bioequivalence and pharmacokinetic studies in Argentina

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LATAM Pharmacovigilance

The team at FP CLINICAL PHARMA can help your company in developing a GOOD PHARMACOVILIGANCE PRACTICES PROGRAM according to your specific needs. THE GOOD PHARMACOVILIGANCE PRACTICES PROGRAM was designed as a quality system based on national and international guidelines and includes the investigation, detection, assessment, validation, monitoring, reporting and archiving of adverse events of the products during commercialization.

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