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About GRP
Why Choose Us
Leadership
Brochure
Careers
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Canada’s Health Canada
United States’ FDA
Brazil
Mexico’s COFEPRIS
Europe’s EMA
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Brazil
TECHNICAL NOTE ABOUT THE NEED FOR SUBMISSION OF CLINICAL TRIALS FOR THE PURPOSES OF REGISTRATION OF HEALTH EQUIPMENT AND MATERIALS
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Brazil
Brazil’s Anvisa: Good Clinical Practices for Inspection Procedures of Drug Clinical Trials
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FRAMEWORK FOR PRIORITY IN THE REGISTRATION, POST-REGISTRATION AND PRIOR CONSENT IN DRUG CLINICAL RESEARCH
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REGULATIONS FOR CLINICAL TRIALS WITH MEDICAL DEVICES IN BRAZIL
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US FDA Guidance: Best Practices in Developing Proprietary Names for Human Prescription Drug Products
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FDA Guidance : Acceptance and Filing Review for PMAs
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