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Introduction to Colombia's Medical Device Approval Process
Colombia has over 48 million residents and is a very strong market for foreign medical device manufacturers. Interested in entering this market? This
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Colombia INVIMA Medical Device Regulatory Approval Process
To market a medical device or IVD, manufacturers must register with the National Food and Drug Surveillance Institute (INVIMA), the country’s medical
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Learn about the Colombian INVIMA regulations which apply to medical devices
Colombia Medical Device Regulations
All Colombia medical device regulations listed below are in PDF format. Please help us maintain this list by reporting outdated or missing documents
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INVIMA - Colombia National Food and Drug Surveillance Institute
The Colombia National Food and Drug Surveillance Institute (Instituto Nacional de Vigilancia de Medicamentos y Alimentos or INVIMA) is regulatory
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Costa Rica medical device & IVD approval process
Medical device manufacturers who want to enter the Costa Rican market need to obtain approval from the Costa Rican Ministry of Health. There are a
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Costa Rica Ministry of Health Overview
The Costa Rican Ministry of Health is responsible for regulating the healthcare industry in Costa Rica. It also acts as the regulatory agency for
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Learn about the Costa Rican regulations which apply to medical devices
Costa Rica Medical Device Regulations
All documents were published by the Costa Rican Ministry of Health and are in PDF format. The Costa Rica Ministry of Health updates their database of
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