Accelerating Your Pre-Clinical Development Trail from early stage proof of concept to large-scale GLP. Our comprehensive services cycle includes: Study design, ethical submission, model selection, protocol writing, drug and medical device performance evaluation, safety & efficacy. Professional accompaniment up to the stage of the submission of the final report to the FDA and or CE.

Our experts committed to addressing all your needs, operating with high reliability and standardization, providing innovative tailor-made solutions, cost and time effective. We have structured a cutting-edge hospital-environment facility, a technology platform, allowing a successful translation of pre-clinical assets towards the clinical evaluation phase.

R&D studies – Preforming innovative activities and studies, supporting our customers to develop new products or improving existing products.

Controlled studies – Our study directors will conduct the trials, write the protocols, prepare test certificates and final reports.

GLP- Good Laboratory Practice – We will conduct the trials, perform and ensure the tests with uniformity, reliability and reproducibility.

Other Complementary Services and Documentation:

Ethical committee approval (Faster than EU)

Protocol Documentation

Tailor- made reporting

General services:

Efficient use Experience & Know- how

Chronic Studies

24h monitoring

Response time (short communication, infrastructure)

Customer tailored participation during conduction

Availability and flexibility

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