Medicinal Products

We can assure all tasks conducting to the marketing authorization, as well as the follow-up of the post-authorisation activities of both human and veterinary medicinal products, including herbal and homeopathic medicines.

Pharmaceutical regulations impact on all areas of drug development, manufacture, control and supply, from the early stages of drug development (including I&D activities, active pharmaceutical ingredients origin), through to dossier submission, approval and maintenance in the market and our expertise cover all these issues. Our company also has a special attention to pharmacovigilance, since it is a crucial regulatory activity, with increasing relevance in the assurance of Public Health protection.

M ao Cubo – Regulatory Consulting can support your company in all stages of the life cycle of medicines.