Product registration
Product regularization with ANVISA
Marketing various types of products in Brazil depends on approval from ANVISA, which has its own dynamic regulations. Obtaining approval requires submitting a set of documents for the Agency's analysis — and that is where CGA comes in.
Pioneer in Brazil
Pioneering consultancy in product registration
We work on the regularization of medical devices — including in vitro diagnostics (IVD) —, food, cosmetics and sanitizers. Our technical team critically analyzes product documents to ensure compliance with all applicable regulations.
Regularization goes beyond drafting and monitoring processes with ANVISA: it includes different types of consulting for the wide variety of regulatory situations clients face on a daily basis.
Portfolio
Examples of services
- Product regularization — complete preparation of technical dossiers
- Compliance with requirements issued by ANVISA (including third parties)
- Regulatory feasibility analysis
- Analysis of formulas and labeling
- Monitoring meetings with ANVISA
- Authorization to exhibit
- Consultation on the need for ANVISA approval
- Requesting copies of files
- Document repository
- Hourly consulting
Technical team
Highlights of our team
- A team of qualified professionals, focused on the best results
- Extensive experience in regulatory advice
- Preparation and monitoring of processes for products of all risk categories and classes
- Serving national and multinational companies of all sizes