DADA Consultancy (DADA) is a highly specialised, independent consulting agency that for over 30 years has been supporting the pharmaceutical industry with human and veterinary medicinal products.

We offer a wide range of services in the fields of pharmaceutical development, clinical support, regulatory affairs, pharmacovigilance, quality assurance, market access and reimbursement in the Netherlands. Together with our sister company ADOH, we can also offer EU batch release service, and GMP/GLP/GDP auditing.

Our Mission

Our aim is to provide state-of-the-art services and to establish long-term partnerships with our clients. Our definition of a service is to help our clients to identify their goals and to develop a plan that will meet the clients’ needs. We have standing partnerships with over 80 international pharmaceutical companies, both human and veterinary. For some of these companies DADA acts as their “virtual private” regulatory affairs or pharmacovigilance department, looking after all required activities. We manage personal data in line with the GDPR requirements, please read our privacy policy.

Our Team

The DADA-team consists of dedicated and highly trained professionals in the pharmaceutical and biomedical field who are supported by a network of external experts, whenever necessary. In this way, DADA is able to provide the best possible services and to find solutions for your challenges.

At DADA we have a passion for detail while maintaining focus on our client’s ultimate goal. We often solve uncommon problems with uncommon approaches, unlocking your data’s full potential. If you are stuck with an issue that seems unsolvable, or are in need for unlisted services, we invite you to contact us. We will give our utmost in helping you out, and in the unlucky chance that we cannot, we will still help you further and find the expert who can.

Our History

Our company was founded in 1984 by Mr Erik Dammers, PharmD, who is enjoying his well-deserved retirement since 2013. DADA has always been based in Nijmegen, the Netherlands, and has since come to an excellent working relationship with the Dutch Medicines Evaluation Board.

In 2014, DADA opened an office in Poland, from where our experts provide assistance in both regulatory affairs and pharmacovigilance.

Since 2007, our team has grown steadily. During the last few years, we grew to a team of over 40 professionals, leading to an expansion of our office in Nijmegen. In September 2020, our second office building was officially opened.

In 2010, DADA joined regulanet ®+, a major network of independent regulatory affairs consultancy firms with members in over 90 countries throughout the world. The services offered by regulanet’s members include all aspects of development, regulatory and market access in their respective countries.


DADA Consultancy is ISO 9001:2015 certified (see our logo below) and we follow our Quality Policy of DADA Consultancy B.V.