YOUR SUCCESS IS OUR GOAL
We are experts in designing and reviewing sterile processing facility designs used for pharmacy compounding and cGMP manufacturing operations, and we have been performing due-diligence compliance audits since 2004.
Our certification and certification oversight services ensures facility designs support testing, and that certification is conducted appropriately and will satisfy regulatory scrutiny.
Our certification and facility related training is expertly designed for certification professionals, engineers, architects, and pharmacists through industry-based groups such as CETA, ASHP, AIHA, USP, the Eagleson Institute, Critical Point, and others.
Certification services for all engineering controls used for production of sterile products and containment of hazardous materials
Reviews and recommendations for facility designs to ensure compliance with appropriate standards
Reviews of existing facilities against regulatory requirements such as USP and FDA guidance documents
World-class in-house training for our certification held by some of the most recognized certification instructors
Experienced cleanroom project management service is available to oversee new installation, repair or renovation projects
Process oversight, includes site visits as needed to inspect the project to ensure design compliances