Regulatory Affairs Consultancy

Partner with Regulatory Affairs Experts for Successful Drug Development

From the early phases of drug development through marketing authorisation, efficient and effective regulatory interactions are essential to your progress and success. These exchanges will not only shape the advancement of your program but also the value of your asset and company. Therefore, it is important to partner with experts, such as a regulatory affairs consultant, who understand the regulatory environment and can act as independent and trusted advisors.

An extension of your team

The regulatory affairs consultants at Venn Life Sciences can work with you, as an extension of your team, throughout the development of your product. By providing timely and competent input on any regulatory concern that may arise, a swift execution of the regulatory strategy is safeguarded. Our regulatory affairs consulting services ensure that you have the support needed to navigate complex regulations and achieve successful outcomes.

Venn Life Sciences can support you in:

Regulatory Affairs Consultancy

Development of regulatory strategy
Regulatory due diligence and gap analyses
Agency interactions with the Food and Drug Administration (FDA), the European Medicines Agency (EMA), and national regulators in Europe
Orphan Drug Designation (ODD) applications