As expert medical device consultants, CiNNAMED provides you with good regulatory and development advice that will save you money and time as you prepare your products for market launch. CiNNAMED will help you understand which regulatory requirements apply, so you can plan ahead to meet requirements cost-effectively and with minimal disruption. We will also find the right collaboration partners for research and development projects for you to speed up your local production and take advantage of tax incentives due to national laws.
CiNNAMED has provided its extensive experience in regulatory affairs to various medical device and pharmaceutical companies with their product registration and approval in Brazil. Through our local partner offices in Brazil and local experts who have established strong relations with their local Ministries of Health, over the years, we can guarantee expert guidance driven to best results.
The following products must register their ANVISA/FDA approval considering the health risk of the product before marketing and manufacturing:
- Medical Devices
- Pharmaceuticals drugs
- Sanitary products
- Food & Supplements