Sanitary Intelligence Consulting
♦ Regulatory Intelligence
We develop business strategies for companies and pharmaceuticals products.
♦ Advisory Board
We act as advisors in public and private companies.
♦ Legalization of companies
We carry out all the steps for legalization of importers, exporters, manufacturers of medicines, medical devices, food, cosmetics, etc. at ANVISA.
♦ Product registration
Preparation of dossiers for medicines, medical devices, cosmetics and food and submission in different regulatory agencies.
♦ Price Registration
Preparation of dossiers and regulatory strategy for price registration of medicines and medical devices at CMED / ANVISA.
♦ Technical Opinions
We develop technical, regulatory and scientific opinions for administrative resources, patents, legal processes, draft laws, public consultations, etc.
♦ Technical-Regulatory Time
Online consulting specialized in regulatory affairs and/ or government affairs at national and international level.
GMP certification, ISO 13485:2016, MDSAP [ANVISA, CE, FDA, etc].
In congresses, events, unions, associations, arguments or defenses in regulatory bodies, Senate, House of Representatives, Comissions , etc.
- Specialized in sanitary regulation within the pharmaceutical industry with national and international operations.
- + 10 years in the market with commercial offices in Brazil and Spain.
- Specialized in legalizing manufacturers, importers, exporters, physcochemical and microbiological laboratories.
- Specialized in different product categories: medicines, medical devices, food (nutraceuticals), cosmetics, etc.
- Its differential is to offer its customers a technical, regulatory, institutional and personalized marketing strategy at the global level (Europe, Latam, USA/FDA, etc.) considering the entire chain involved in order to ensure the compliance of the company.
- Over the years we have developed a methodology using the regulatory strategy to ensure compliance of our customers.