Vita Consulting provides Regulatory Affairs advice for pharmaceutical industries supporting the registration and post registration of medicines, from the preparation to submission of the dossier to the regulatory body. Our consultants are qualified to fully comply with the sanitary regulations of the Brazilian market (ANVISA) and other Latin American countries. Our mission: Advise the regulatory affairs department of our clients to optimize workflow, ensure the maintenance of current products and contribute to the expansion of their portfolio with new drug registrations. More information about our services at www.vitaraconsulting.com