PHARMA R&D

HBP pharmaceutical development experts are able to fully execute and/or support the development of any finished dosage form, formula or process, as well as the transfer of a developed product from small-scale GMP production area or scale-up to a manufacturing facility.

With our pragmatic and creative development mentality, we deliver what a client needs. We perform best by exploring together the motivations behind their request.

Our pharmaceutical formulation services are supported by strong in-house analytical, dissolution and excipient characterization platforms.
HBP do offer the typical ad-hoc analytical and pharmaceutical development services, we often perform full development programs where we take up projects right from start and deliver product solutions custom-made to the needs and interests of our clients. Our approach is fully integrated and combines hands-on pharmaceutical and analytical development work (formulation & CMC) with high-standard regulatory, intellectual property and market access support.

Our expertise and capabilities are centered around the development of value-added generic drugs, life cycle management of branded drug products, and complex formulation.

R&D Operation
Pre-Clinical Formulation
Prototype Development
Characterization Studies
Analytical Support
Compatibility Studies
Stability Studies

Transfer to GMP
IMPD
Analytical Method Transfer
CMO Selection
Scale-up

HBP offer local and inTernational regulatory affairs and support, as well as professional translations services, eCTD dossiers preparation and Package Leaflets user testing for readability.
We are operating in several regions(Mena),in Czech Republic, Hungary, and in other EU countries.HBP