ANOVA CRO is a specialist Biometrics Contract Research Organisation.  We are clinical data-focused experts with over 20 years of experience working with Pharmaceutical, Biotechnology and Medical Device companies.

With a close-knit local team, all based in the Czech Republic, we do not use third-party contractors meaning that our clients are assured quality of provision on their projects.

At ANOVA CRO, we practice a ‘quality over quantity’ approach, and we are generally seen as an integrated part of our client’s team.  We have the flexibility to support all of the steps in drug development, from initiation and protocol development to submission of study results to regulatory authorities in requested format.

ANOVA CRO have an excellent record of supporting approval for a range of novel drugs regulatory authorities including the FDA, EMA and PMDA where we have collected, analysed and submitted study data in CDISC format.

ANOVA CRO is able to deliver a wide range of services including:

Biostatistics
SAS Programming
Clinical Data Management
CDISC Services 
Medical Writing

To discuss your project and to find out how ANOVA CRO can support email Radka Štěpánová via info@anova-cro.com

ANOVA CRO

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