Blog Archive

Viable environmental monitoring provides critical information towards understanding the relative cleanliness of the sampled environment. Typically, viable airborne and surface data is collected to…

How would you define a high-quality testing service? Quality means conformance to requirements; and the requirements are dependent on the related industry. This makes quality a subjective concept as…

HEPA filters are sold in a variety of models and configurations, including with or without injection and testing ports. As HEPA filter leak testing involves upstream challenge of the HEPA filter with…

  USP has postponed the official dates of the below chapters from December 1, 2019 until further notice: · <795>: Pharmaceutical Compounding – Nonsterile Preparations · <797>:…

Why test CDA or CGS systems? Compressed dry air or compressed gas systems are critical utilities in your clean environments. CDA or CGS systems may be used in process applications directly or…

Validation of temperature-controlled chambers is a critical component of a robust process and/or facility qualification plan. Validation includes Installation Qualification (IQ), Operational…

USP <797> lays the foundation of standards for compounding sterile preparations. According to USP, “…<797> helps to ensure patients receive quality preparations that are free from…

Here at Technical Safety Services we are dedicated to the highest quality of compliance and safety for our clients, their processes and the people they serve.  Our services are used by over 11,…