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CLASS II BIOSAFETY CABINET
Due to recent industry developments, our company has assembled a division to assist sterile compounding pharmacy facilities comply with all USP 797 requirements.
Our staff includes pharmacists, design engineers, cleanroom contractors, NSF and CETA accredited certifiers.
We have the latest information regarding the National Association of Boards of Pharmacy (NABP) announcements of their action plan and inspection process. The NABP will be coordinating inspections with the resident board of pharmacies. State specific instructions have been sent to each board of pharmacy office. Additional inspections will be planned to follow for all types of pharmacy compounding facilities.
Clean Air Flow is equipped with the knowledge and expertise to offer consulting services, as well as any facility upgrades necessary for meeting all requirements for compounding pharmacies.
About the CETA accreditation:
For years the profession has requested the Controlled Environment
Testing Association (CETA) to develop a certification for professionals
working in our field. As registered CETA cleanroom professionals,
Clean Air Flow staff have proven expertise in sterile compounding facility
testing and validation.
Board of Pharmacy inspection surveys are requesting documentation of
USP 797 Consulting:
Today, facilities we service have to be more vigilant than ever before when contamination control
issues are critical to preparing sterile products. Clean Air Flow provides viable air and surface sampling to monitor for all types of potential contamination, both bacterial and fungal. Our company uses state of the art monitoring equipment and expert reference laboratories to provide test results.
We also provides remedies to control contamination issues.