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Pharmaceutical Drugs

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.

Pharmaceuticals

⟶ from preclinical to clinical (Phase I, II, III) to market commercialization.

Drug Development

Drug Development

New pharmaceuticals are required to be manufactured to high quality standards before they can be placed on the market. We support your from drug discovery to pre-clinical and clinical testing.

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Regulatory Procedures

Regulatory Procedures

There are various procedures for drug registration, depending on the type of the product and your intended route to market. QbD’s consultants will walk the right path with you.

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Submissions

Submissions

Applications for marketing authorisation must be accompanied by the required documentation. QbD will help you to get your documents right.

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eCTD

eCTD

Compiling eCTDs can take years of training, industry immersion and regulatory study. QbD is your competent partner for electronic submissions.

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Why opt for QbD Austria?

10+ years of experience

Benefit from our team of highly qualified consultants.

Full life cycle support

Full support from pre- to the post-marketing phase.

Global presence

QbD operates globally, at QbD Austria with a special focus on Europe (EU) and China.

Customer satisfaction

Constant evaluation, transparency and clear objectives.

Contact us

Talk to an expert

Contact us for more information or to request a free, no-obligation proposal.