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Who We Are
M&C MED is a consultancy/manufacturer/importer company specialized in the approval/regularization of health products, together with INMETRO and ANVISA. Our focus is to assist our customers/partners in the product registration/registration process (equipment and materials), where we have a manufacturing unit, which allows us to offer a better cost and shorter process time. We are located in Sete Lagoas – MG and our unit has all the necessary licenses to offer the services below for health products in risk class 1, 2, or 3.
We have a multidisciplinary team, with more than 20 years in the market and professionals (former ANVISA consultant) in the GGTPS area and specialists in product projects.
Mission and Vision
At M&C MED, our mission is to be the main partner for companies in the healthcare sector in the journey of registering medical products with ANVISA. We are committed to providing high quality, efficient and reliable services, ensuring that our clients achieve their registration objectives effectively and within the strictest regulatory standards.We understand the crucial importance of medical product registration for the safety and well-being of patients, as well as the commercial success of our customers. Therefore, we dedicate our efforts to simplify and speed up the registration process, offering specialized support at every stage, from preparing documentation to obtaining final approval.Our commitment to excellence and professionalism allows us to provide a personalized service tailored to the individual needs of each client. We always seek to exceed expectations by offering innovative solutions, expert guidance and ongoing support throughout the entire registration process.At M&C MED, we believe that our customers' success is our success. Therefore, we work tirelessly to ensure that each medical product registered through our services meets the highest standards of quality, safety and effectiveness, contributing to the advancement of health and well-being of society as a whole.Join us on our mission to make the medical product registration process more accessible, efficient and transparent. At M&C MED, we are here to help you achieve your goals and make a difference in the world of healthcare.
CERTIFICATE OF GOOD PRACTICES
The Certificate of Good Practices is the document issued by Anvisa certifying that a given establishment complies with procedures and practices established in the Agency's specific standards. M&C Med is certified for the production and industrialization of class l, ll and lll health products.
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FAQ
What types of services does M&C Med offer?
- Registrations of medical, dental, and aesthetic procedure products and equipment;;
- Manufacturing of medical, dental, and aesthetic procedure products and equipment;
- Storage;
- Importation;
- Distribution;
- After-sales support (technical assistance and user support);
- Techno-surveillance (monitoring of products on the market in compliance with RDC 665 of March 30, 2022)
What types of businesses does M&C Med serve?
- Manufacturers, distributors, hospitals, and other interested parties in commercializing medical, dental, and aesthetic procedure products and equipment;
- Distributors and retailers who wish to market products with their own brand.
What are the advantages for my business?
Reduction of costs and time for registrations, providing agility to insert products into the national market.
What is the investment to obtain the advantages of being an M&C Med partner?
Request a proposal from our consultants by email l comercial@mecmed.com.br
Is this partnership safe for my business?
Yes. All partnerships are carried out through a contract with clauses aligned between the parties to guarantee the legal security of the parties involved.
Rua Afonso Viana De Paula, 183A
Eldorado -Sete Lagoas - MG - 35.702-165 comercial@mecmed.com.br +55 (31) 3773-1067Segunda a Sexta das 08:00 as 18:00
Eldorado -Sete Lagoas - MG - 35.702-165 comercial@mecmed.com.br +55 (31) 3773-1067Segunda a Sexta das 08:00 as 18:00
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