Services for operations in Brazil.

Medicines and pharmaceutical ingredients

Regulatory planning for pharmaceutical manufacturing, import, distribution, storage and transport.

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.

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

Assess additional authorizations for activities involving substances or products subject to special control in Brazil.

Assess sanitary requirements for logistics, storage and transport, considering product categories and contractual responsibilities.

Align documentation and operating routines and assess the work needed for compliance and certification projects.

TECNOVISA

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