Menu
The aim is to evaluate which products or medical supplies are more cost-effective than similar ones on the basis of treatment, efficacy and safety.
Study whose objective is to see the feasibility of a potential study. Feasibility studies give us clarity on whether a study can be developed in the country or not.
We provide major support in the search for researchers, review and customization of essential documents and regulatory submissions to the corresponding entities.
Pharmacovigilance studies are activities related to the detection, evaluation, understanding and prevention of adverse drug effects or any other drug-related problem.
Clinical research studies aimed at demonstrating efficacy and/or safety.
These studies are governed by Good Clinical Practices (GCP).
In these studies there is no direct intervention with the research subject. Their objective is to "observe" the usual medical practice in different types of studies in different pathologies and/or treatments.
In these studies there is no direct intervention with the research subject. Their objective is to "observe" the usual medical practice in different types of studies in different pathologies and/or treatments.
In these studies there is no direct intervention with the research subject. Their objective is to "observe" the usual medical practice in different types of studies in different pathologies and/or treatments.
In these studies there is no direct intervention with the research subject. Their objective is to "observe" the usual medical practice in different types of studies in different pathologies and/or treatments.
PCR drafts the information that regulatory agencies usually request about a product that has been submitted to obtain its sanitary registration. Most of the documentation is governed by the rules of the European regulatory body (EMEA).
We provide audits of clinical research and pharmacovigilance studies to drugstores and/or pharmaceutical laboratories.
PCR provides Project Manager services in different types of studies, mainly in clinical trials. Project management is of utmost importance for the execution of the study in any of its different phases.
At PCR we are in charge of developing in vivo therapeutic equivalence studies to demonstrate the interchangeability of drugs submitted to the ANM.
Copyright © 2023 | PCR. Contract Research Organization.
