ACliRA Consulting GmbH

ACliRA's MISSION

We want to turn your clinical development into a success story for both, your company and the patients depending on your therapeutic approach.

ACliRA's AMBITION

Clinical development of new pharmaceutical or device products must be directed by competent experts to ensure highest quality of data with reasonable spending of resources.

ACliRA's PEOPLE

Our people act with great responsibility for your asset and your company value, and leverage all skills to achieve your goals in budget and time.

Successful clinical development. Period.

Clinical Development

Whether full blown clinical development plans or individual clinical trials — we can support you to find the best strategy to demonstrate efficacy and safety of your pharmaceutical or medical device product.

Due Diligence Activities

We provide detailed and due-diligence proof assessment of asset’s strength and weaknesses as well as opportunities and threats (SWOT).

Regulatory Support

We offer professional and reliable support for regulatory interactions, at a reasonable budget. As a registered SME with EMA, we can offer competitive pricing for scientific advice procedures for all clients.

Strategic Advice

We give you strategic advice for your clinical development activities, incorporate views from clinical experts and implement most recent scientific results. Simply, we increase the chances for a successful completion of your clinical development.

What can we do for you?

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Looking for answers?

Unsure about hurdles or pitfalls in the development of inhaled products for respiratory or infectious diseases? Our vast experience in pulmonary and infectious disease medicine combined with sound knowledge of aerosol science will give you reliable answers and identify potential gaps to achieve the best outcome of your clinical development.

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