According to the regulatory norms of any country it is necessary to register the product before its commercialization and distribution. The main objective of this is to allow the regulatory agency to ensure and guarantee the supervision, surveillance and quality control of the product.
Instituto Latinoamericano de Biotecnología MECHNIKOV with a mission to bring high-quality medicines to every country in Latin America and Caribbean,
With this motive, last year Institute MECHNIKOV iniciated the process of vaccine registration in Republic of Guatemala, which is mapped to be a country with high potentials for comercialization of such products.
In the process of product registration, many technical, scientific and legal documents were presented that are approved by the National Regulatory Agencies and Ministries to obtain the sanitary registration.
On 13 of October 2020 we obtained the Sanitary Registration for Influenza Vaccine (Split Viron) Inactivated.
With Obtaining the sanitary registration of the VAIF vaccine, which is manufactured in Central American region, guarantees access to the population of Guatemala to an affordable and high quality vaccine.