Performance Qualification Services

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.