Brazil
Showing 33–48 of 49 results
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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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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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TECHNICAL REGULATION: ESSENTIAL REQUIREMENTS FOR SAFETY AND EFFICACY OF MEDICAL DEVICES
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TECHNICAL REGULATION: THE REGISTRATION OF MEDICAL PRODUCTS AT ANVISA: ALTERATION, REVALIDATION, OR CANCELLATION (ANNEXES)
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TECHNICAL REQUIREMENTS FOR AUTHORIZATION OF PERSONEL CARE PRODUCTS, COSMETICS AND PERFUMES
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TECHNICAL REQUIREMENTS FOR CHILDREN’S PERSONAL CARE PRODUCTS, COSMETICS AND PERFUMES
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TECHNICAL REQUIREMENTS FOR INSECT REPELLENT (COSMETIC PRODUCTS) REGISTRATION
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TECHNOVIGILANCE RULES APPLICABLE TO REGISTRATION HOLDERS IN BRAZIL
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THE REGISTRATION OF VITAMINS, MINERALS, AMINO ACIDS AND PROTEINS CLASSIFIED AS SPECIFIC MEDICINES FOR ORAL USE
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