We offer a variety of services to our clients including
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.
REGULATORY ISSUES
We help you classify, register and host your medical devices with ANVISA in Brazil and other countries. We'll finde the best option for you to either own your personal registration or enter into a collaboration with a hosting partner.
LEGAL ISSUES
Business creation strategy, legal representation of your company, accounting and taxation services are part of our portfolio making sure that you take the most efficient and safe track into your desired market.
DISTRIBUTION / SALES
Finding the best and especially trustworthy partner to be your partner is often one of the biggest challenges in foreign territory. We will make sure to identify companies and professionals matching your requirements and objectives.
RESEARCH AND DEVELOPMENT
Our years of experience in the fied of industrial academic research and development projects for healthcare technology enable a unique support for our clients in setting up grant applications, project timelines, organization and processes as well as the identification of funding opportunities and tax advantages.
REGULATORY ISSUES
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
- Cosmetics
- Sanitary products
- Food & Supplements