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Dec 12, 2024
Regulatory Intelligence and the Role of Clinical Studies
Oct 17, 2024
Anvisa publishes the list of active ingredients of medicines with registration requests under analysis
Sep 12, 2024
We must support Anvisa
Aug 30, 2024
Post-registration of medicines – opportunities and challenges
Aug 12, 2024
Clinical Research Law: A Historic Regulatory Milestone for Clinical Trial with Human Beings in Brazil
Aug 5, 2024
GGBIO task force: solution or palliative?
Jul 11, 2024
Anvisa: 25 years with many stories to tell
Jun 27, 2024
Challenges in the development and registration of biosimilars
Jun 17, 2024
Anvisa's General Management of Medicines releases the 2023 Management Report
May 31, 2024
Real-world studies for drug registration: ANVISA guidelines
May 9, 2024
Impact of Reliance on the Regulated Sector
Apr 18, 2024
Clinical Research involving Advanced Therapies: impacts of RDC nº 836, December 2023 - ANVISA / Brazil
Feb 7, 2024
Find out about Anvisa's priorities for the next biennium
Nov 21, 2023
RDC 753 - New Regulatory Framework for the Registration of Synthetic Drugs.
Nov 6, 2023
What are the challenges in ensuring access to high-cost medicines?
Oct 26, 2023
WHAT ARE THE STEPS FOR OBTAINING AUTHORIZATION FOR CLINICAL STUDIES IN BRAZIL?
Oct 9, 2023
Important circumstances for the submission of drug registration in Brazil
Sep 29, 2023
What are the topics of interest and ANVISA’s availability for meetings?
Aug 22, 2023
What is the purpose of registration submission guide, based on data from scientific literature?
Aug 4, 2023
Six suggestions for a successful Advisory Board
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