AlphaBeta Pharma offers Development Consultancy & Due-diligence services for pharmaceutical & biotech companies, governmental bodies and academic institutions regarding drugs and medical devices and technology transfer. This includes either review or planning of:
- Preclinical and toxicology
- CMC work
- Clinical development plans
- Regulatory strategy and dossier review
- Pharmacovigilance system
- TPP and marketing strategy
- Clinical / non-clinical overview
We present various options for our services, from fully contracted-out to fully contingent, non-fee basis, instead sharing a portion of future commercial revenues. We commonly cover development/clinical trials costs and can inject funds directly to carry out critical proof-of-concept or technology development work. We can also help you to raise funds and even help with placement.
All of these services are provided through a one-point-contact via a dedicated Project Manager assigned for your project and sometimes located even in your own country.
Please click here to request more information or to arrange for a possible free face-to-face meeting