Brazil Pharmaceuticals
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Brazil’s Anvisa : Good Manufacturing Practices (GMP) for Radiopharmaceutical Medicines
$50.00 Add to cart -
Brazil’s Anvisa: Classification Criteria and Procedures Of Non-Prescription Medicine Medication
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Brazil’s Anvisa: Conducting Clinical Trials with Medicines in Brazil
$350.00 Add to cart -
Brazil’s Anvisa: Good Clinical Practices for Inspection Procedures of Drug Clinical Trials
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Brazil’s Anvisa: Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients(API)
$400.00 Add to cart -
Brazil’s Anvisa: Good Manufacturing Practices (GMP) guidelines
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CRITERIA FOR CONDUCTING STABILITY STUDIES FOR ACTIVE PHARMACEUTICAL INGREDIENTS AND NON-BIOLOGICAL DRUGS
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FRAMEWORK FOR PRIORITY IN THE REGISTRATION, POST-REGISTRATION AND PRIOR CONSENT IN DRUG CLINICAL RESEARCH
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GOOD MANUFACTURING PRACTICES FOR EXPERIMENTAL DRUGS USED IN CLINICAL TRIALS
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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
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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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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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THE REGISTRATION OF VITAMINS, MINERALS, AMINO ACIDS AND PROTEINS CLASSIFIED AS SPECIFIC MEDICINES FOR ORAL USE
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