1. Generating the CTD filed Total Development Plan of a new project from cell lines to animal models, Regulatory Toxicology and the following Clinical Trials from
phase I to phase IV
2. Consulting service during all phases of pre-clinical and clinical development, including preparation of the necessary documents (e. g.: IMPD, IB, Study Synopsis)
3. Scientific due diligence of companies and projects to provide decision support for the acquisition of funds
4. Assistance to raise funds

5. Expert Opinion for drug industry and VC