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What Sets Us Apart

At Quantus, we understand the distinct challenges faced by pharmaceutical companies. Our tailored approach merges cutting-edge technology with profound expertise in pharmaceutical manufacturing and laboratory processes, providing services that not only comply with but surpass regulatory requirements. Our commitment goes beyond being a service provider; we are your strategic partner dedicated to driving growth, ensuring quality, and fostering innovation.

In the dynamic and highly regulated pharmaceutical landscape, maintaining momentum is critical. Quantus is your trusted ally, offering a comprehensive range of specialized services designed to support drug development and production while guaranteeing compliance and operational efficiency.

Ensuring Integrity in Pharmaceutical Equipment Services

Onsite Services

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    Calibration Services

    Quantus delivers on-site NIST Traceable Calibration for life sciences lab equipment, manufacturing process systems, and supporting utilities.

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    Validation (CQV) Services

    Nationwide commissioning, qualification, and validation services for life science facilities. Quick delivery off-the-shelf and custom protocols.

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    Preventive Maintenance

    Improve lab equipment safety and reliability. Our maintenance program is minimally invasive, flexible services, with same-day reporting.

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"I've found that Quantus is the best certifier to work with in this region. Their paperwork is straightforward and easy to understand. We've presented their reports to the FDA multiple times with no issues, and the FDA has acknowledged that Quantus reports require little review and are known to be top-notch. It was a pleasant surprise to find Quantus working at my new company."

John, QuVa

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We Have Answers To Your Problems

Frequestly Asked Questions

What calibration services does Quantus provide for pharmaceutical equipment?

Quantus offers comprehensive onsite calibration services tailored for the pharmaceutical industry. Our NIST Traceable Calibration ensures that lab equipment, manufacturing process systems, and supporting utilities meet rigorous accuracy and reliability standards. These services help maintain compliance and enhance product integrity throughout the pharmaceutical development and manufacturing processes.

How does Quantus support pharmaceutical companies in meeting regulatory compliance for cleanroom environments?

Our cleanroom certification services are designed to ensure that pharmaceutical manufacturing environments meet all regulatory standards, including ISO classifications. Quantus performs detailed assessments and validations to certify that cleanrooms maintain the required cleanliness levels, which are crucial for product safety and efficacy. Our approach helps companies stay audit-ready and manage risks effectively.

How does Quantus assist with environmental monitoring and validation services, including EMPQ, for pharmaceutical facilities?

Quantus offers comprehensive environmental monitoring and validation services, including our specialized Environmental Monitoring Performance Qualification (EMPQ) services, to ensure that pharmaceutical facilities operate within required regulatory frameworks.

Our EMPQ services are designed to elevate cleanroom integrity through expert validation against global standards, cutting-edge microbial and particulate detection, and tailored solutions to meet specific needs.

We conduct thorough risk assessments to identify and mitigate contamination risks, ensuring compliance with FDA and global regulations. These efforts help secure manufacturing excellence and product safety with our streamlined and effective EMPQ approach.

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