Introducing QHUB
Learn how our QHUB Dashboard streamlines document retrieval, service requests, and more...
![QHUB_Illustration_4](https://goquantus.com/hs-fs/hubfs/QHUB_Illustration_4.png?width=1278&height=844&name=QHUB_Illustration_4.png)
Learn how our QHUB Dashboard streamlines document retrieval, service requests, and more...
Elevating Cleanroom Standards, Enhancing Product Safety, and Ensuring Quality at Every Step
Essential services for life sciences facilities aiming to ensure the highest standards of sterility and safety. Our approach targets the heart of microbial risk, offering comprehensive assessments and solutions tailored to your unique environment. By identifying critical areas prone to contamination, we lay the groundwork for a robust sterility assurance program that aligns with global regulatory expectations.
Our EMPQ services go beyond basic compliance, setting a new standard in environmental monitoring. We not only identify the most effective monitoring points within your facility but also implement a strategic EM program that's both robust and representative of your operational risks. Trust Quantus, Inc. to elevate your cleanroom integrity, ensuring your manufacturing processes are safeguarded against contamination, thus protecting product safety and patient health.
EMPQ refers to the specialized process of assessing and ensuring that a cleanroom or controlled environment meets the required standards of cleanliness and control. This involves testing for particulates and microbial contamination, ensuring that the environment is suitable for its intended use, especially in pharmaceutical or biotech production.
EMPQ is crucial because it ensures that your cleanroom environment adheres to the necessary regulatory and compliance standards, such as those set by the FDA and other international regulatory bodies. This not only helps to prevent product contamination, ensuring product safety and effectiveness, but it also helps to protect your operations from costly downtime and liability issues.
Our EMPQ services are designed to go beyond basic compliance requirements. We provide expert validation against global standards, risk assessment, cutting-edge microbial and particulate monitoring, and tailored solutions specific to your needs. Our approach is more comprehensive, targeted, and strategic, ensuring a higher level of cleanroom integrity and operational risk management.
Absolutely. We understand that each industry and facility has unique requirements. Our EMPQ services offer custom solutions that are developed to fit the specific needs of your cleanroom and manufacturing processes, whether you operate in pharmaceuticals, biotechnology, medical device manufacturing, or any other field requiring controlled environments.
We pride ourselves on regulatory mastery. Our team stays up-to-date with the latest FDA and global regulations to ensure that your cleanroom environment is always compliant and audit-ready. We provide comprehensive documentation and support throughout the process to make certain that your facility meets all the necessary standards for operational excellence.
I am very pleased with the services provided. The technicians are exceptional to work with, and the customer support team is incredibly responsive and accommodating. The pricing offers excellent value for the services provided.
Century Therapeutics Drew
The technicians here do an outstanding job. I truly appreciate the responsiveness of the customer support team and their proactive approach to scheduling.
Ellume Ken
Everything is going great with the services. The technicians are top-notch – professional, honest, and very solid in their work. They provide excellent communication and feedback.
RegenXBio Blake
Working with Quantus to resolve the disorganization of previous 3rd party reports. I have received positive feedback on the work Quantus is doing. We're looking forward to a meeting with the top management and business development teams to gain more feedback and develop additional controls.
Christiana Care James
NIST Traceable Onsite Field Calibration Services ensuring Precision and Reliability for your Laboratory Equipment, Manufacturing Operations, and Supporting Facilities and Utilities Equipment.
Our service ensure your compliance to ISO 14644 for design, construction, validation, and operating cleanrooms and related HEPA Filtered Equipment. Enhancing product quality and safe environments.
Over a Decade of Excellence in CQV: Delivering Nationwide, Validation Solutions for GMP Facilities, Process Systems, Laboratory Equipment, and Temperature Mapping Services.