About us
A warm greeting to all our readers. Hoping that you are all in good health, we introduce you the first entry of this blog, that greets us in a unique time for this generation: a pandemic. This unprecedent situation has had a titanic impact not only in economics, but also in health-related matters: it has given us the chance to see the importance and variety of health products, that include not only medicines and medical devices; it has forced us to pay close attention to scientific research and it has reinforced the importance of all healthcare professionals, that directly or indirectly, are involved in improving our health.
In that matter, it is also important to mention that the interest of diving into the pharmaceutical industry has also raised significatively, in areas such as manufacturing, importing and/or marketing health products, as well as in opening establishments related to storage or commerce of health services and health products.
With that in mind, a lot of questions come to mind. What is the regulatory agency that authorizes manufacturing or commercialization in Mexico? What are the steps I need to follow in order to be able to sell health products? What permits or authorizations do I need to sell foreign health products? And for domestic products?
To help you solve these questions, you can rely on Regulatory HS, your commercial ally. As regulatory affairs experts, we will explain the requirements and procedures established by Comisión Federal para la Protección contra Riesgos Sanitarios- regulatory agency in Mexico- in order to import health products and be able to sell them in national territory or to start different establishments related to commerce, manufacturing, or storage of health products, as well as those related to providing health services. We have the answers to the questions that you may have, with years of experience behind us.
Until next time,
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