Our approach combines technical expertise, reliable infrastructure, and competitive pricing to help you achieve your goals.
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.
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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We combine compliance, infrastructure, and operational efficiency to help you reduce risks, improve performance, and move forward with full regulatory clarity.
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.
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.
Our quality and traceability systems ensure consistent batches, reduced variability, and more predictable delivery times.
With 41 years of experience serving domestic and international companies, we provide comprehensive support, clear communication, and defined timelines.
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.
We review your project confidentially to determine the best strategy.
We evaluate efficient routes that reduce travel time, improve performance, and ensure stability.
We scale up your process with precision, traceability, and a focus on quality.
Our development expertise translates into robust and reproducible processes, ensuring quality, control, and consistency at an industrial scale.
We produce consistent batches backed by regulatory compliance and robust quality controls.
At Interquim, we offer:
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.
Yes. We are FDA-certified and have experience working with companies in various countries.
Yes. We provide consulting services from initial development through commercial production.
From pilot and clinical batches to commercial-scale production, tailored to your project’s needs.
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.
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.
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.