Phase IV involves the safety surveillance and an ongoing technical support regarding a product, after it receives the authorization to be marketed.

Use the expertise and knowledge of Latin American CRO MMATISS to fulfill your post-approval needs. Our services cover all the process from the planning of data collection and data analysis, until the stage of reporting.

Also you can use our services to plan and perform trials oriented to support marketing claims that will highlight the particular benefits that your medicinal products have, to offer to the consumers.