acora pharma consulting

acora pharma is your specialist in drug regulatory affairs – for all pre- and post-approval activities.

We assist pharmaceutical companies in bringing new products onto the market. Due to our international activities we are familiar with global as well as national requirements and legislations.

Furthermore, we provide support over the entire product life-cycle in order to guarantee compliance with continuously increasing regulatory requirements and the implementation of changes requested by our clients.

Our clients’ satisfaction is our motivation.

On-site support is also possible. Please contact us!


As Qualified Person according to the EU Directive 2001/83/EC (“Sachkundige Person” according to § 15 of the German Drug Law), we are qualified to offer support to pharmaceutical companies in production, quality control and batch release according to all drug regulations.


Our clients profit from our long-standing experience and high level of quality standards.

Our overall goals are to obtain authorization of your application in the quickest time, to reduce the risks and costs as well as to improve the quality and safety of your drug product.