QbD Austria offers you the complete package to bring your pharmaceuticals to the European and Chinese markets. We support you during the whole product life cycle, from pre- to the post marketing phase.
Our consultants offer extensive regulatory affairs knowledge and expertise to support your team or insource complete regulatory affairs projects – all in an efficient and pragmatic manner.
⟶ from preclinical to clinical (Phase I, II, III) to market commercialization.
Why opt for QbD Austria?
Contact us for more information or to request a free, no-obligation proposal.