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Feb 9, 2021
Unraveling the Abbreviated Development Path
Feb 9, 2021
Publication of the Public Consultation for the review of RDC 200 - what is new?
Feb 9, 2021
NEW REGULATORY FRAMEWORK OF API
Feb 9, 2021
What is the purpose of clinical research on health products?
Feb 9, 2021
Incremental innovations - what are the financial benefits?
Feb 9, 2021
Incremental innovation: 5 suggestions that can contribute to your success
Feb 9, 2021
What are the new expectations for the development of incremental products and medicines?
Feb 9, 2021
INCREMENTAL INNOVATION: How to prepare for the changes that will come with the revision of RDC 200
Feb 9, 2021
COVID-19: What facilities is ANVISA providing at this time of crisis?
Feb 9, 2021
Why are 24% of drug registrations still rejected?
Feb 9, 2021
Cannabis: challenges and opportunities
Feb 9, 2021
API, BPF and drug dossier - How to align the processes to ensure success in registration?
Feb 9, 2021
NEW API REGULATORY FRAMEWORK: Will ANVISA and international manufacturers be prepared?
Feb 9, 2021
Publication of the new API regulatory framework: what is essential to know?
Feb 9, 2021
What is important about the new regulatory framework for good manufacturing practices?
Feb 9, 2021
Cannabis for therapeutic uses: is this a new market?
Feb 9, 2021
Outcome of the RDC 200 Review Working Group meeting - 02/05/20
Feb 9, 2021
Cannabis: the rules of the new regulation system.
Feb 9, 2021
Everything you need to know about the new rules for Drug Renewal.
Feb 9, 2021
Clinical studies for health devices: 5 value tips
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