In the absence of specified standards governing compressed air quality testing in the pharmaceutical manufacturing process, it is often best to use site-specific compressed air testing programs for Points of Use (POU). This may be the most assured way to produce valid, repeatable testing results that will reinforce your site’s quality.
TRI recommends a Baseline Test, Direct Product Contact, Indirect Product Contact, United States Pharmacopeia (USP), the European Pharmacopeia, or the ISO 8573 air standard for Points of Use (POU). We can also test nitrogen, oxygen, argon, carbon dioxide, custom compressed air specifications and more.
The compressed air used in the manufacturing processes should be evaluated by a competent technical individual to determine the appropriate requirements to protect the safety of the employees and the integrity of the products. We suggest a baseline test before validation. TRI has experienced validation and qualification Dealers that can work with your requirements and staff to produce the validatable systems, descriptions and documents you need to move your project forward.
The quality of the independent laboratory you use is critical to ensuring that your facility’s efforts to achieve compressed air best practices are optimized. Understanding your true compressed air quality needs and utilizing high-quality laboratory support are keys to air quality compliance in manufacturing. Click here to know more about #iso 8573 compressed air testing.
TRI recommends a Baseline Test, Direct Product Contact, Indirect Product Contact, United States Pharmacopeia (USP), the European Pharmacopeia, or the ISO 8573 air standard for Points of Use (POU). We can also test nitrogen, oxygen, argon, carbon dioxide, custom compressed air specifications and more.
The compressed air used in the manufacturing processes should be evaluated by a competent technical individual to determine the appropriate requirements to protect the safety of the employees and the integrity of the products. We suggest a baseline test before validation. TRI has experienced validation and qualification Dealers that can work with your requirements and staff to produce the validatable systems, descriptions and documents you need to move your project forward.
The quality of the independent laboratory you use is critical to ensuring that your facility’s efforts to achieve compressed air best practices are optimized. Understanding your true compressed air quality needs and utilizing high-quality laboratory support are keys to air quality compliance in manufacturing. Click here to know more about #iso 8573 compressed air testing.
No comments:
Post a Comment