You have great medical products and want to approve and market them worldwide? Especially in European countries and Brazil, this expansion can be quite challenging and frustrating due to numerous regulations and standards, if you are not familiar with the culture and the local conditions. At the same time, testing and approval in Brazil is very inexpensive, with a given infrastructure and almost the same standards. This is why Sobel Consult exists. We help medical device manufacturers with international regulatory affairs and quality management to establish and market their products worldwide. Based in Brazil, our international experts support you with their decades of experience in every step of the product life cycle: 🔸 Quality Management 🔸 Product Documentation 🔸 Project Management 🔸 Regulatory Affairs 🔸 Local Representative Service Our goal is to keep your company compliant in the most efficient way. This is achieved through modern software tools, highly qualified experts and competitive pricing structures.