Clipping of news on Brazilian Culture, Law and Citizenship
26/04/2012
This article was translated by an automatic translation system, and was therefore not reviewed by people.
Anvisa will test a new way to perform its public consultations. The goal is to offer society a more efficient way to participate in the consultations and position themselves in relation to the proposed regulation. To this end, the Agency will use an electronic form in which the participant may enter their considerations on the system directly to items in the proposal it deems appropriate.
The publicity and transparency of the public consultation process will also be valued. With the new system, you can monitor what are the items of the proposal under discussion that receive more suggestions and which sectors of society participate.
In this new model, the participant does not need to send the document, simply record the suggestions which will be sent directly to the responsible area of ANVISA. The participants of the public consultations may also make changes to your text after sending the contribution, provided that the period of participation is still open. The system under test will use a tool already developed by the Ministry of Health, FormSus, which is maintained by Datasus and serves as a basis for research on health.
A new form of public consultation it will be tested with a proposed regulation approved Tuesday by the board of ANVISA, during its meeting open to the public. This is the norm for the Certificate of Good Manufacturing Practices for Pharmaceutical Excipients, which are substances used to make drugs, but that does not have pharmacological activity. The proposal must be published in the coming days in the Official Gazette (DOU) and will be in consultation for 60 days.
At the same meeting, the directors also approved a public consultation on the Criteria for Grouping in Product Families For In Vitro Diagnostic Use For the Purpose of Registration and Records. Currently, there is no definition about what these products can be grouped into families, which complicates the analysis of the process and increases the number of corrections in the documents. The consultation period will be 30 days from publication in the Gazette.
Carlos Augusto Moura - Press / Anvisa
Source: ANVISA
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This article was translated by an automatic translation system, and was therefore not reviewed by people.