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Cleanroom, Cleanroom Certifications, and Cleanroom-CQV
Cleanrooms are vital in ensuring that life sciences products—such as pharmaceuticals, medical devices, and biologics—are manufactured in environments that minimize the risk of contamination. Even…
Cleanroom validations for aseptic manufacturing
Validation of cleanrooms for aseptic manufacturing is crucial to ensuring the quality and safety of pharmaceutical and biopharmaceutical products. Aseptic processing involves handling and manufacturing…
Cleanroom Validation & IQ OQ PQ Qualifications Complete Guide
Cleanroom commissioning and qualification are critical processes that ensure the integrity and functionality of controlled environments. These processes involve thorough planning, testing, and documentation to…
Cleanroom Trainings
What are Cleanroom Trainings? Cleanroom trainings are structured educational programs designed to equip personnel with the knowledge and skills necessary to work in controlled environments…
Cleanroom Smoke Studies
Cleanroom smoke studies are critical to assessing the airflow, cleanliness, and overall performance of controlled environments such as cleanrooms. Contamination control is essential for pharmaceuticals…
Cleanroom Panels for Biologics Facilities
Cleanroom panels for biologics facilities are critical to maintaining the necessary environmental conditions to produce, store, or handle biologics products. These panels are designed to…
Cleanroom Gowning & Qualifications: Navigating the Essentials of Cleanroom Gowning for Beginners
A cleanroom is a controlled environment to maintain shallow particulate contamination. It is typically used in manufacturing and scientific research environments where even small amounts…
Cleanroom Environmental Monitoring Performance Qualification (EMPQ)
Cleanroom Environmental Monitoring Performance Qualification (EMPQ) Overview: The Cleanroom Environmental Monitoring Performance Qualification (EMPQ) is a critical part of the validation process to ensure that…
Cleanroom Documentation
The Cleanroom Documentation Package (CDP) is a critical set of documents that ensures cleanrooms meet industry standards and regulations for use in controlled environments, such…
