News & events

A cleaning validation demonstrates a pharmacy, hospital, or outsourcing facility’s cleaning procedure is effective and consistent in cleaning equipment and compounding surface areas. The Food and Drug Administration (FDA) expects firms to have written procedures (SOP’s) detailing the cleaning processes used for various pieces of equipment.

According to Center for Disease Control and Prevention (CDC), over 8 million US healthcare workers are exposed to hazardous drugs (HDs) every year. Drugs classified as hazardous include cancer therapy, antiviral drugs, hormones, and bioengineered drugs.   More than 12 billion doses of HDs are handled by US providers each year. Anyone handling HDs is at risk

According to the FDA, ensuring data integrity is an important component of industry’s responsibility to ensure the safety, efficacy, and quality of drugs. ARL Bio Pharma has GMP software that controls our laboratory’s instruments and generated data. This software complies with 21CFR Part 11 as it relates to electronic records. All data is locked down