Pro-Val SPLtd.

is a full-service CRO. The staff manages feasibilities, site selection, study start-up, regulatory affairs, monitoring, and overall study management according to all applicable regulations.


Our aim is to provide the best possible CRO services to small and medium-size pharmaceutical sponsors. Our organization offers consistency and experience, at competitive prices. We have experience in phase I, II, III studies for big multinational pharmaceutical companies, medium-sized sponsors from Europe, USA, and the Middle East, studies for academic consortiums and investigator-initiated trials (IITs), sponsored by the European Community.
We are performing postauthorization (phase IV) and scientific research studies. Our focus is on expertise, personalized approach, accuracy, prompt response to sponsors’ demands and quick delivery of services. We have accumulated experience with electronic CRFs, patient’s assessment, and the rest of the ancillary methods utilized in multi-center international trials, to improve assay sensitivity. We have a database on a network of capable investigators. Being a rather small and closely-knitted organization we can do all that in a very straightforward manner lacking clumsiness, red-tape procrastination, and procedural rigidity but retaining the needed depth of experience and knowledge to bring your projects to a successful completion.
Such an approach defines our relationship with our customers, regardless of the size or complexity of the project. Sponsors could rely on either our end-to-end services or a single service provided in several sites and countries.
Our recruiting and management abilities make us a secure candidate for handling complex studies. Call us today!

We invite you to inquire about our capabilities and services and are always ready to review your needs and provide you with an estimate of what we can accomplish on your behalf.

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