Consulting and Services

REUTERS International Regulatory Consulting & Services offers highly qualified consultancy for registration projects in Central and South America, Africa, and Asia, especially to small and medium-sized pharmaceutical companies.

Based on a sound strategic and operational know-how in all matters of regulatory affairs and a broad, detailed knowledge of valid guidelines for submissions in Central and South America, Africa, and Asia, we can offer you consultation for the successful filing of your dossiers and for controlling the submission process in these international areas.


Following a detailed interview with your company about your business objectives and the countries in which you intend to obtain approval for your pharmaceutical products, we will help you draw up a concept for registration that is especially suited to your requirements and interests.

We will review your dossier for its suitability for approval in the target countries and inform you of any changes or additional documents necessary for a successful submission.

It is our aim to find the best regulatory strategy for the registration of your products.

We cooperate with local business partners, consultants, CROs, and companies who will help support submission to the Regulatory Authorities in the target countries.

As a result of this “all-round service”, we consider ourselves a competent and reliable business partner for supporting you through a successful submission and outcome for marketing authorizations and your international regulatory affairs.



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