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CLASSIFICATION CRITERIA AND PROCEDURES OF NON-PRESCRIPTION MEDICINE MEDICATION
$50.00
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CRITERIA FOR CONDUCTING STABILITY STUDIES FOR ACTIVE PHARMACEUTICAL INGREDIENTS AND NON-BIOLOGICAL DRUGS
$300.00
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FRAMEWORK FOR PRIORITY IN THE REGISTRATION, POST-REGISTRATION AND PRIOR CONSENT IN DRUG CLINICAL RESEARCH
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GMP FOR ACTIVE PHARMACEUTICAL INGREDIENTS (API)
$400.00
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GOOD CLINICAL PRACTICES INSPECTION PROCEDURES FOR DRUG CLINICAL TRIALS
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GOOD MANUFACTURING PRACTICES FOR EXPERIMENTAL DRUGS USED IN CLINICAL TRIALS
$150.00
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GOOD MANUFACTURING PRACTICES OF RADIOPHARMACEUTICAL MEDICINES
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GOOD MEDICINES MANUFACTURING PRACTICES GUIDELINES
$550.00 $450.00
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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
$400.00
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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
$300.00
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REGULATION FOR CONDUCTING CLINICAL TRIALS WITH MEDICINES IN BRAZIL
$350.00
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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
$30.00
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THE REGISTRATION OF VITAMINS, MINERALS, AMINO ACIDS AND PROTEINS CLASSIFIED AS SPECIFIC MEDICINES FOR ORAL USE
$50.00
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