Services for operations in Brazil.

Support for Anvisa technical requests

Review the official request, the process history and the available evidence to define a consistent response strategy.

TECNOVISA

A scope tailored to your operation.

We consider the product category, business activities, establishment and documentation available for assessment.

The proposal identifies deliverables, responsibilities, dependencies and any third-party work or official fees.

Tecnovisa carries out the agreed regulatory work and follow-up according to the scope of the engagement.

Support for medical device market access in Brazil, based on intended use, classification and technical documentation.

Evaluate the regulatory impact of a new address, changes to company information or expansion of authorized activities.

Organize recurring regulatory needs, portfolio changes and ongoing obligations through a clearly defined service agreement.

TECNOVISA

Discuss your company’s regulatory needs and the scope of a suitable engagement.