
The subject is on the agenda of the 6th Public Meeting of the Collegiate Board of Directors (Dicol) of 2025, scheduled for Wednesday (10/08)

Submission of registrations, videos, and requests for confidentiality ends at 11:59 pm this Friday (5); item revising rules for cannabis products will be defined at the Dicol meeting on December 10

Marcelo Mario Matos Moreira assumes as substitute in the Fourth Board, filling the vacancy of the former rapporteur of the review of RDC 327

Decision postpones vote on new rules for cultivating varieties with low THC content; new date for analysis has not been defined yet

Change may authorize cultivation by companies under strict control, with a limit of 0.3% THC; measure complies with a decision from the Superior Court of Justice (STJ) related to cultivation regulation.

Proposal aims to regulate the performance of non-profit entities in a controlled experimental environment, using the Regulatory Sandbox model to comply with STJ decision

Anvisa directors meet this Wednesday (28) to discuss the update of medicinal cannabis regulations; learn how to follow

Public consultation proposal for the review of RDC No. 327/2019 will be evaluated by the Collegiate Board on December 19, 2024

Anvisa directors meet this Wednesday (28) to discuss the update of medicinal cannabis regulations; learn how to follow

Revision of RDC 327 allows the compounding sector to produce derivatives, while individual importation by individuals remains under old rules and will be analyzed separately

Proposal in the review of RDC 327/2019 to RDC 660/2022 divides opinions and raises doubts about access and judicialization

The Brazilian Association of Pharmaceutical Inputs Industry trusts that the request for a view by director Thiago Campos will result in a more in-depth analysis, maintaining the expectation of concluding the regulatory framework in January 2026

Rapporteur Rômison Mota advocated for changes impacting imports via RDC 660; new rule prioritizes national products when there is equivalence

The item revising RDC 327/2019 reaches a decisive week at Anvisa, and the sector awaits to know if the topic will proceed to a vote or be postponed once again

According to Filipe Campos, from Close-Up International, the market could expand even further with rule updates and greater medical adherence

Thiago Campos advocates for the extension of the regulation deadline and reinforces the importance of social listening in the process

Public consultation allows society to express opinions on the agency's priorities for the next two years; preliminary list does not include cannabis

Update of the RDC included in the Regulatory Agenda 2024-2025 is expected for next year

Rômison Rodrigues Mota leaves the position after a request for review delays the norm's vote; the topic will return to the regulatory agenda for 2026-2027

Entity reinforces that personalized preparations are essential when industrialized products do not meet clinical needs