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RegisterANVISA Approval [Regulatives / Guidelines]
Dear shiv,
it's different from the FDA.
The center(s) performing the study must follow ANVISA's rules (http://www.anvisa.gov.br/eng/legis/resol/103_03rdc_e.htm), must be inspected (http://www.anvisa.gov.br/eng/bio/form_bio.doc), and renew their status anually (http://www.anvisa.gov.br/eng/bio/form_renewal.rtf). After approval of the protocol by the local IEC, the study may be performed.
Only if your protocol deviates from ANVISA's standards (e.g. if you want to perform at multiple dose study in order to reduce variability for HVDs), I would strongly recommend contacting them before.
good luck!
Hermann Rotter
it's different from the FDA.
The center(s) performing the study must follow ANVISA's rules (http://www.anvisa.gov.br/eng/legis/resol/103_03rdc_e.htm), must be inspected (http://www.anvisa.gov.br/eng/bio/form_bio.doc), and renew their status anually (http://www.anvisa.gov.br/eng/bio/form_renewal.rtf). After approval of the protocol by the local IEC, the study may be performed.
Only if your protocol deviates from ANVISA's standards (e.g. if you want to perform at multiple dose study in order to reduce variability for HVDs), I would strongly recommend contacting them before.
good luck!
Hermann Rotter
Complete thread:
- ANVISA Approval shiv 2006-01-25 06:39 [Regulatives / Guidelines]
![[Mix]](https://static.bebac.at/img/mix.png "open in Mix view")
- ANVISA Approval H_Rotter 2006-01-25 12:31
- ANVISA Approval shiv 2006-01-27 08:14
- ANVISA ApprovalH_Rotter 2006-01-27 14:00
- ANVISA Approval shiv 2006-01-27 08:14
- ANVISA Approval H_Rotter 2006-01-25 12:31
Ing. Helmut Schütz