Anvisa to use external analysis to register medical devices

Person registrating a medical device

Anvisa to use external analysis to register medical devices

Anvisa (National Health Surveillance Agency) is simplifying the registration of medical devices with a new Normative Instruction. An advance in regulatory confidence, following WHO recommendations for rapid access to health technologies. Read more here

If you need more information about regulatory issues in the pharmaceutical industry and healthcare, ELS can certainly help.

Please do not hesitate to contact your local ELS consultant or via email info@elssolutions.pt

ELS Group

ELS Group brings together a team of highly specialized professionals with proven experience in regulatory frameworks and compliance in the pharmaceutical field.

Strategic consulting for the pharmaceutical, healthcare, food, and medtech industries.

Rely on experts to support your regulatory decisions and accelerate the growth of your products safely and efficiently.

Strategic consulting for the pharmaceutical, healthcare, food, and medtech industries.

Experts in pharmaceutical consulting, regulatory strategy, and market access to support your company with safety, compliance, and efficiency. Talk to a consultant.