RDC 753 - New Regulatory Framework for the Registration of Synthetic Drugs.
What are the challenges in ensuring access to high-cost medicines?
WHAT ARE THE STEPS FOR OBTAINING AUTHORIZATION FOR CLINICAL STUDIES IN BRAZIL?
Important circumstances for the submission of drug registration in Brazil
What are the topics of interest and ANVISA’s availability for meetings?
What is the purpose of registration submission guide, based on data from scientific literature?
Biological and biosimilar medicines - development and commercialization challenges
What was the impact of the pandemic on clinical studies?
Clinical research in Brazil - regulation is important and urgent!