Our experience combined with a thorough understanding of the analyzed processes allowed us to create an offer of comprehensive services.
The scope of services offered as part of preclinical and clinical trials of medicinal products includes:
- consulting research and development projects for new medicinal products, including biopharmaceuticals, especially at the pre-clinical stage,
- scientific understanding of research topics (defining the goals and methods of operation as well as the possibility of conducting research), developing research programs,
- planning, designing preclinical in vitro and in vivo tests and clinical trials for various medicinal substances and pharmaceutical forms,
- assistance in choosing the right research center,
- supervision and monitoring of the course of work in the selected center,
- preparation of research documentation (medical writing),
- comprehensive implementation of bioavailability and bioequivalence studies (from developing assumptions to issuing a final report in accordance with international standards),
- consulting and giving opinions on documentation submitted for registration, especially in the field of bioavailability and bioequivalence tests.