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APIs with signature Solutions that streamline and strengthen your supply chain Our approach combines technical expertise, reliable infrastructure, and competitive pricing to help you achieve your goals. APIs Development, optimization, and manufacturing of APIs (Active Pharmaceutical Ingredients) in accordance with international standards. We have stable and efficient processes in place so you can move forward with greater confidence.

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More CDMO/CMO We support your project from development and/or technology transfer through to commercial production. Our team works with you to ensure scalable, stable, and well-documented processes.

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Quickly access the most important sections of our site. Your project, backed by real capabilities We combine compliance, infrastructure, and operational efficiency to help you reduce risks, improve performance, and move forward with full regulatory clarity. Contact us Regulatory compliance Our certifications and strict adherence to international standards (including FDA guidelines) provide you with the regulatory assurance you need to move your project forward without risk, with auditable processes and reliable documentation at every stage.

Adaptable infrastructure We have the capacity to handle quantities ranging from grams to tons, using versatile equipment that can accommodate different volumes and levels of complexity. This allows you to move forward with clarity and without operational constraints. years of experience 0 Quality Our quality and traceability systems ensure consistent batches, reduced variability, and more predictable delivery times. Extensive experience With 41 years of experience serving domestic and international companies, we provide comprehensive support, clear communication, and defined timelines.

With sales in more than 50 countries worldwide 0 A clear process that gives you visibility from the start We work with you through a transparent and well-organized process to ensure that every stage—from evaluation to manufacturing—proceeds safely, efficiently, and with seamless communication.



Technical and regulatory assessment We review your project confidentially to determine the best strategy. Process development and optimization We evaluate efficient routes that reduce travel time, improve performance, and ensure stability.

Scaling

We scale up your process with precision, traceability, and a focus on quality.

Validation

Our development expertise translates into robust and reproducible processes, ensuring quality, control, and consistency at an industrial scale. Commercial manufacturing We produce consistent batches backed by regulatory compliance and robust quality controls.

Beneficios QUALITY + COMPLIANCE + AGILITY + FDA CERTIFICATION + EXTENSIVE EXPERIENCE + RELIABILITY + FLEXIBLE INFRASTRUCTURE + OPERATIONAL EFFICIENCY + A SMOOTH AND ORDERLY PROCESS + Trust built on compliance and technical expertise At Interquim, We Offer GMP compliance.

Strategic location with FDA certification.

We tailor our services to the needs of your project.

Multipurpose infrastructure for development, scaling, and regulated commercial production. Move your project forward with a reliable team Contact us Get your questions answered and move forward with confidence Here you’ll find clear answers about how we work, what services we offer, and how we can support your project from the early stages through to commercial production. Does Interquim work with international companies?

Yes. We are FDA-certified and have experience working with companies in various countries. Can you support projects in their early stages? Yes. We provide consulting services from initial development through commercial production.

What production scales do you handle, and what is the maximum capacity of your manufacturing operations? From pilot and clinical batches to commercial-scale production, tailored to your project’s needs. What CDMO/CMO services and capabilities do we offer for your project?

At Interquim, we offer CDMO/CMO services for development, scale-up, and contract manufacturing. We have R&D; facilities, a pilot plant,



and multipurpose production facilities to support you from initial synthesis through commercial manufacturing, ensuring quality, regulatory compliance, and competitive timelines. What do you need to evaluate my project?

We only need general information about the molecule, the stage of the process you are currently in, and the estimated volumes. With this information, we can assess the feasibility and provide you with better guidance. All information is treated with the utmost confidentiality.

Why do pharmaceutical companies trust our quality and compliance standards? Because at Interquim, we combine over 40 years of experience with cGMP-compliant operations, FDA certification, and robust quality systems that ensure traceability, safety, and consistency. Our ongoing audits and comprehensive regulatory documentation support reliable compliance for clinical and commercial projects.

What APIs (Active Pharmaceutical Ingredients) does Interquim manufacture? At Interquim S.A. de C.V., we manufacture Active Pharmaceutical Ingredients (APIs) for human and veterinary use, complying with international quality standards and regulatory requirements. Our commercial API portfolio includes strategically important molecules that have already been validated at the industrial level, including: Key APIs In The Interquim Portfolio Fosfomycin Tromethamine

Rifaximin

Dexmedetomidine (base and hydrochloride)

Atipamezole Hydrochloride

Diacerein In Addition, We Manufacture Other Specialized APIs, Such As Amikacin Sulfate

Detomidine

Medetomidine

Cobamamide

Hydroxocobalamin

Pyrimethamine

Rifapentine Our catalog is complemented by APIs under development and CDMO/CMO projects, tailored to each client’s technical, regulatory, and volume requirements. To learn more about availability, presentations, or to start a custom project, we invite you to contact our technical team directly. Interquim is a Mexican pharmaceutical and chemical company with over 41 years of experience in the development and manufacture of APIs.

It is FDA-inspected and committed to the highest standards of quality and compliance.

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