Managerial procedures required to obtain the Good Manufacture, Distribution, and Storage Practice Certificate
June 30, 2021
Anvisa issued the Resolution of the Collegiate Board of Directors (RDC) 497/2021, in which it establishes the managerial procedures required to obtain the Good Manufacture Practice Certificate and the Good Distribution and/or Storage Practice Certificate. The objective of this resolution is to …
How to add health product use instructions in Anvisa’s portal?
June 17, 2021
Anvisa requires the attachment of health product information during their registration in the regulating body’s portal. After the effectuation of the RDC no 431/2020, which enforces the upload of use instructions on Anvisa’s digital portal related to medical device notification or registration …