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Passarini Regulatory Affairs has been working for more than 10 years with ANVISA and has highly knowledgeable professionals with vast experience in product registration.
We are able to provide all support in each step for your product registration (FDA, CE Mark, ANVISA and others), ISO 9001 / ISO 13485, RDC 16/2013 (BGMP – Good Manufacturing Practices) and Hosting Services as well.
Our HQ’s in Brazil with 2 offices. In addition, we’ve operational offices in Lisbon-Portugal, in Miami-USA and Shanghai-China.
Let us know if you are interested in our services.
For more information send us an e-mail: [email protected]
Passarini Regulatory Affairs