Discover our full CRO services

ExperTrials is a european full-service Contract Research Organization (CRO) providing 

clinical trial support to Biotech and Medtech startups to launch their innovative drug or medical device.

We provide experienced Clinical Research professionals and teams worldwide to monitor all aspects of your trial, using the most powerful clinical management tool in the industry.

Our experienced Quality Assurance (QA) team will monitor every steps of your clinical trials to ensure that the whole study is conducted in compliance with all guidelines, local and international regulations.

For assistance with regulatory affairs, our local Clinical Research Consultants (CRC) are highly-experienced and well-trained.

We plan and monitor patient safety throughout your clinical trial and guarantee that the proper safety procedures are in place.

Are you interested in running a study in the EU and you are not established in the EU?

ExperTrials is able to be your legal representative in EU, we handle all the European Legal Complexities and you focus on your trial.

Our medical monitors are professional medical doctors with several years of experience in pharmaceutical medical positions. We offer clinical trial oversight, strategic consulting and safety support.

At ExperTrials, we work with preferred partners in data management and biostatistics in order to advise and support all aspects of data capture and analysis from protocol and eCRF design through to database lock.

With the Functional Service Provider (FSP) model, you can pick and choose which services to outsource in order to benefit from our expertise

The Market Access function is present throughout the life cycle of the product even if the core of its activities will be in Phase IIb and Phase III. The aim of the function is to successfully launch a product ensuring optimal price and reimbursement from the payer

Founded in 2011 and based in Villeurbanne (France), ExperTrials conducts international trials from phase I to phase IV, driven by a diligent market access analysis. We have significant experience in both pre-approval and post-approval trials.

We know that your timelines are extremely tight in order to get the data needed to support the next round of funding and take the
next step in the advancement of your clinical development programme. We have the flexibility to respond to changes through all
phases of your project.

Our objective is to become an extension of your team by keeping a transparent and regular communication during each of your
project steps.

We have extensive experience from all aspects of the global drug development industry. Our Project Managers have an average of
10 years of experience and are well equipped to work alongside our client teams to develop strategy, maneuver challenges, and
drive teams to meet and exceed study goals.
Our expert team works closely with you to tailor the best solution for each project and to deliver clinical trials of the highest quality.
We understand that each customer has unique needs and we work to design innovative, custom solutions across the full drug
development life cycle.

Our primary concern at ExperTrials is the patient. We do not consider the patients as a data source, but as the drivers of our

We are proud to deliver services that will contribute to improve millions of human lives, using a patient-centric approach.

Do you need some additional information concerning our CRO services ? Get in touch with us

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Le Patio – 35/37 rue Louis Guérin – 69100 Villeurbanne, France

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