Brazil Health Authority
“INSPECTION PROCESSES AND REQUIREMENTS TO VERIFY THE GOOD MANUFACTURING PRACTICES OF MANUFACTURERS OF ACTIVE PHARMACEUTICAL INGREDIENTS, HEALTH PRODUCTS OF RISK CLASS III AND IV AND MEDICINES” has been added to your cart. View cart
Showing all 4 results
-
Anvisa Regulation: Technical regulation of imported goods and products for health surveillance into Brazil
$250.00 Add to cart -
INSPECTION PROCESSES AND REQUIREMENTS TO VERIFY THE GOOD MANUFACTURING PRACTICES OF MANUFACTURERS OF ACTIVE PHARMACEUTICAL INGREDIENTS, HEALTH PRODUCTS OF RISK CLASS III AND IV AND MEDICINES
$400.00 Add to cart -
PROCEDURES FOR THE TRANSFER OF REGISTRATION OF PRODUCTS AND CLINICAL TESTING SUBJECT TO HEALTH SURVEILLANCE NOTIFICATION
$250.00 Add to cart -
REGISTRATION, CONTROL, AND MONITORING OF THE PRODUCTS AND THE CONDITIONS FOR THE OPERATION OF COMPANIES SUBJECT TO SANITARY LICENSING, WITHIN THE SCOPE OF HEALTH SURVEILLANCE
$50.00 Add to cart