Showing 129–144 of 155 results
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RDC No. 36/2015 RESOLUTION ON THE RISK CLASSIFICATION, THE SYSTEMS OF NOTIFICATION CONTROL, REGISTRATION AND LABELING REQUIREMENTS AND INSTRUCTIONS FOR USE FOR IN VITRO DIAGNOSTIC DEVICES AND THEIR INSTRUMENTS
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Record Filing Requirement of Medical Device Master Files
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REGISTRATION FOR GENERIC, SIMILAR, SPECIFIC, DYNAMIZED, HERBAL AND BIOLOGIC MEDICINAL PRODUCTS (SIMPLIFIED PROCEDURE)
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REGISTRATION OF RADIOPHARMACEUTICALS OF MANUFACTURED IN NATIONAL TERRITORY
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REGISTRATION PROCESS OF BIOLOGICAL PRODUCTS
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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
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REGULATIONS FOR CLINICAL TRIALS WITH MEDICAL DEVICES IN BRAZIL
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REGULATORY REQUIREMENTS FOR GOOD MANUFACTURING PRACTICES (GMP) FOR MEDICAL DEVICES AND IN-VITRO DIAGNOSTICS IN BRAZIL
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REGULATORY REQUIREMENTS FOR NOTIFICATION AND REGISTRATION OF CLASS I AND CLASS II MEDICAL DEVICES IN BRAZIL
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Remote Inspection
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REQUIREMENTS FOR PROVING THE SAFETY AND HEALTH BENEFITS OF PROBIOTICS FOR USE IN FOOD
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RULES FOR PROVIDING INSTRUCTIONS FOR USE OF HEALTHCARE PRODUCTS IN NON-PRINTED FORMATS
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RULES FOR SUBCONTRACTING: PRODUCTION STAGES, CONTROL ANALYSIS FOR QUALITY CONTROL, CONTROL OF TRANSPORT AND STORAGE OF MEDICINES AND BIOLOGICAL PRODUCTS
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SPECIAL PROCEDURE FOR THE CONSENT OF CLINICAL TRIALS, GOOD MANUFACTURING PRACTICES CERTIFICATION AND NEW DRUG REGISTRATION FOR THE TREATMENT, DIAGNOSIS OR PREVENTION OF RARE DISEASES
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TECHNICAL NOTE ABOUT THE NEED FOR SUBMISSION OF CLINICAL TRIALS FOR THE PURPOSES OF REGISTRATION OF HEALTH EQUIPMENT AND MATERIALS
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TECHNICAL NOTE ON HEALTH PRODUCTS LABELING INFORMATION
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