Visanco emerged as a result of the great academic and professional experience of our founder, Antonio Osvaldo, who worked for over 20 years in the Ministry of Health and PAHO/WHO in regulatory actions, training and decentralization in health surveillance for states and municipalities.
Thus, in 1997, we constituted Visanco as a tool to unveil the regulatory world, its laws, decrees, ordinances and resolutions, with the sole purpose of translating, simplifying and transmitting to this legal framework to stakeholders, as well as the procedures, proceedings and understandings of the regulatory agents.
Over the years, we have incorporated into our group highly qualified professionals who have contributed to the continuity of the excellence of the services provided by Visanco.
We are a company recognized nationally and internationally, not only for our capacity to generate technically and scientifically well-founded solutions, but also for the condition of strategically evaluating the projects of interest to our clients under the legal, political, economic and social frameworks.
For us, challenges and overcoming are routines we experience on a daily basis. There are countless contacts, doubts, innovative and creative projects in which we perform in a professional, ethical and transparent way, with a high level of commitment and always respecting the rules and current legislation and, especially, the health of the population.
Providing the best technical and strategic solutions for the health segment, enabling a complete understanding and application of current legislation. In order to do so, we value transparency and ethical relationships with our clients and public agencies.
Becoming the largest Company in health regulatory matters and the one that best aggregates knowledge and solutions for our customers, by understanding their wishes and needs, contributing to the availability and innovation of products and services in the health area.
Respect, commitment, proactivity, ethics, spirit, transparency, professionalism.
Advising and training companies and governments, both at national and international levels in the health field, providing technical and strategic solutions for their complete regularization, as well as products before the competent bodies.
We provide the necessary support for the regularization of ingredients and products at ANVISA and MAPA, performing activities such as
Institutional Relationsand Market Access are essential points for the development of new business in health.
Acting in the Regularization of Companies and Products with the competent bodies of the Ministry of Health (ANVISA):
With the publications of Resolutions RDC 09/2015 (Medicines) and RDC10/2015 (Products for Health), the clinical trials conducted in Brazil, which will serve to subsidize applications for product registration, need to be evaluated and granted by ANVISA.
Enjoy the convenience of having your documents filed or withdrawn in Brasilia, at the place and day indicated by you!
Summit e Exposição sobre inovações, tecnologias e tendências para ingredientes e nutrição com foco em saudabilidade, funcionais e nutracêuticos, para...
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