SciSafe has developed over 60 Standard Operating Procedures (SOPs) that govern all functions within the business. A robust Quality Plan and Corrective And Preventative Action (CAPA) system modeled after the FDA required systems (21cfr parts 210 & 211) for pharmaceutical manufacturers make Scisafe a valued partner in every stage of drug development and distribution.

SciSafe is cGMP compliant. Its electronic systems including sample inventory, sample monitoring, chain of custody, document control and training are 21cfr part 11 compliant. SciSafe is anticipating attaining CAP accreditation in 2017.