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Follow the rest of the guidelines to finalize the approval. They will also be able to be answered via voice call via wi-fi, with a scheduled time per message, using the same applications.

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Password reset request. As of October 17, there have beenscientific publications related to the disease worldwide.

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To meet national and regional information needs and provide transparency to studies, the Brazilian Registry of Clinical Trials ReBEC - an online platform for experimental and observational studies - disseminates various research on a specific disease or drug that is underway in Brazil, through data that does not always find space in scientific journals.

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The formula is based on Phtalox technology, a compound initially created to treat bad breath and improve gum health, revealed the magazine Galileu. Attach mandatory ethics committee documentation and submit the form.

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The puts Brazilian production in the 11th position in the world ranking. Brazil is part of the restricted group of countries that have published the most studies on covid since the beginning of the new coronavirus pandemic.

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In order to conduct these studies in Brazil, participating institutions must resort to their own Ethics Committees or partner institutions, which analyze research according to the National Ethics and Research Council Conep and the National Health Surveillance Agency Anvisa. Fast-track can reduce the normal approval period for clinical trials to less than 48 hours, favoring the transparency of research and reducing bench time for society to test and use medicines, vaccines and other health innovations.

The existing fast tracks - zika, dengue, yellow fever and malaria - and the attendance to other studies will not be interrupted.

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All studies that evaluate the clinical, pharmacological or side effects of drugs in humans are called clinical trials. Up. Of these, 4, are ed by researchers working in the country.

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The so-called fast track may reduce the normal approval period, from up to a few weeks, to less than 48 hours. Choose the type of service: chat, audio recordings or voice call by appointment.


It uses the Dimensions platform, an international database with daily updates. Send a message with your name and.

It is neither necessary nor recommended to send your password. The objective is to shorten the time between the beginning of the research, the testing and the arrival of medicines, vaccines and other innovations to society. For English, in case of difficulty, use the Google Translate tool or another free translation tool.

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Scientists around the world will have quick access to modeling studies already underway, avoiding rework and favoring cooperation. Dear user, Our review and support services are suspended today. In the last five years, Brazil has been appearing as the 13th country that has published the most scientific articles and research reviews", said Canuto. Please leave a message in the chat, if possible with a telephone, so that we can return after the restoration of services.

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We are at a very good stage of development. Register a single service on your Whatsapp. It is ahead of that produced by countries like Holland, Switzerland and Japan.

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Fast track users will receive online support through four dedicated phone lines, using messages in free apps like Telegram or Whatsapp, or even through the chat provided by the platform. Coordinator Dra. Register or and normally fill out the forms in Portuguese and English. Your form will be revised in both languages.

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A reviewer will answer you. The platform has more than 3, approved records, all of which have been validated by the most important scientific journals in the world and open to public consultation and is the only primary record in the world in Portuguese recognized by the World Health Organization. In addition to the hour operating system with automated e-mail messages every day, human service will be expanded, starting earlier, at 8 am, and going until 8 pm. Managed by Fiocruz and publicly owned, the service has free access, free of charge for anyone who wants to register or consult approved records.