Services for operations in Brazil.

Regulatory consulting for medicines and pharmaceutical ingredients

Assessment of pharmaceutical projects, documentation and regulatory maintenance, with a scope tailored to the product category.

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.

Plan company authorization for medicines and pharmaceutical ingredients, considering activities, facilities and any special-control requirements.

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

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.