Technical rigor
Every deliverable is grounded, referenced and standardized according to the applicable regulation.
About
Specialists in regulatory consulting for health products
CGA Consulting specializes in technical consulting for Regulatory Affairs and Quality Management Systems. We work alongside medical device, dental, aesthetics and related industries, conducting ANVISA registrations, INMETRO certifications and CE Mark and FDA processes.
Our team is made up of specialists with hands-on experience in complex and constantly changing regulatory environments. We have expanded our scope by also acting as Registration Holder in Brazil for foreign companies.
Our founder
Claudia Azevedo
CEO and founder of CGA Consulting
An Industrial Pharmacist with an MBA in projects, quality and industrial production, Claudia has over 20 years of experience in national and multinational pharmaceutical and medical device industries.
Certified as a Lead Auditor for Medical Device industries under ISO 13485:2016, she serves as an Expert Member at ABNT and as PRRC (Person Responsible for Regulatory Compliance), leading regulatory compliance projects in Brazil and abroad.
- Industrial Pharmacist — MBA in projects, quality and production
- Lead Auditor ISO 13485:2016
- Expert Member at ABNT
- PRRC — Person Responsible for Regulatory Compliance
- Over 20 years in national and multinational industries
Our principles
Business vision
Regulatory solutions designed for the client's reality and time to market.
Constant updating
Real-time monitoring of national and international regulatory changes.