CRO & preclinical consultant solutions I Versa Biomedical

Tailored preclinical development solutions

We provide ad hoc solutions for our sponsors/clients through in vivo studies using the swine model.

Whether you are embarking on drug discovery, developing a medical device, conducting safety and toxicity studies, or preparing for clinical trials, we are here to support you on every step of the way.

01 / Biopharma preclinical trials

Versa Biomedical has experience in conducting in vivo preclinical tests for drug development, under GLP certification where needed. We support our partners from the very beginning of the preclinical phase through the development process, ensuring compliance with global regulatory requirements.

Proof of concept

We run preclinical studies that are essential to demonstrate the true validity of an approach.

Efficacy studies

We conduct tests to assess the efficacy of test items, tailoring the study plan to meet our sponsors’ specific requirements.

PK / TK

We run every kind of pharmacokinetic and toxicokinetic studies.

Preclinical toxicology studies

We investigate the response of drugs to evaluate their toxicity and safety.

Innovative services and solutions to take your preclinical studies further

At Versa Biomedical, we are dedicated to help you advance in your research and development goals.

Ad hoc solutions for unique needs

We are ad hoc solvers, with a precise custom-made process, covering specific and unique needs.
Powered by a solution-driven aim

We are experts in our field, rigorous and proactive, always willing to find the best solution
We are fully GLP certified

And compliant with the guidelines issued by ICH, ISO13485, EMA, ISO 10993, FDA and other relevant health authorities.
Committed to quality assurance

We prioritize quality at every stage of the development process, ensuring reliable results that meet regulatory expectations.