Access to innovative therapies

Our Rare and Orphan Diseases Unit is dedicated to facilitating access to innovative and highly specialized therapies for patients living with low-prevalence conditions, often without available treatment alternatives in the country.

Comprehensive Strategy for Rare Diseases

We focus on developing commercial and regulatory strategies for high clinical value molecules that address real needs within the Peruvian healthcare system. While many of these diseases appear during childhood, our approach is comprehensive and covers all age groups.
Our outlook includes the incorporation of new therapies from international laboratories committed to the treatment of rare and orphan diseases, meeting the highest quality standards.

Cutting-edge treatments

The unit focuses on next-generation products, including monoclonal antibodies and molecules developed with advanced biotechnology, aimed at conditions with high clinical and social impact. Our commitment is to ensure these treatments reach those who need them most, within a regulated, transparent, and constantly evolving framework. In the current context, where Peru has recently regulated the approach to rare diseases, this unit remains in continuous regulatory and technical updating, identifying opportunities to efficiently respond to current provisions and facilitate the entry of new therapies into the country.

Clear Advantages of Our Service

Access to
Therapies

The unit enables patients with rare diseases to access state-of-the-art treatments, even when no options are available locally.

Comprehensive
Strategies

Specific commercial and regulatory solutions are developed for high-value molecules, with a cross-cutting approach that spans all age groups and addresses the country’s real needs.

Regulatory
Compliance

We work with advanced biotechnology (such as monoclonal antibodies) within a regulated framework, staying up to date with Peruvian regulations to facilitate the safe entry of new therapies.

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Pharmacovigilance is the science and activities related to the detection, assessment, understanding, and prevention of adverse reactions or any other health problem associated with medicines or vaccines.

Pharmacovigilance seeks to ensure that the benefit-risk balance remains favorable throughout the entire life cycle of a medicine, that is, from the time it is authorized until it is withdrawn from the market or its production is discontinued.

Pharmacovigilance seeks to ensure that the benefit-risk balance remains favorable throughout the entire life cycle of a medicine, that is, from the time it is authorized until it is withdrawn from the market or its production is discontinued.

Pharmacovigilance involves various public health activities of risk analysis and management that contribute to the rational use of medicines.

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