Regulatory Affairs

Based on our local up-to-date knowledge in the regions we are working in, we guide you through a smooth approval process for your trials.

Ecron Acunova’s regulatory consultant group provides clinical development planning, positioning of strategies, preparation of dossiers, and submission of study-related documents to regulatory authorities and ethics committees.
Ecron Acunova’s regulatory experts are experienced in effective and diplomatic liaison with regulatory bodies in support of a wide variety of indications and represent/support you in meetings with regulatory agencies.

For more information, please see our website.