Lives are at stake

To ensure the safety and continued effectiveness of medicinal products, hospitals and laboratories must store drugs, vaccines and samples at specific refrigeration and freezer temperatures. QA programmes are increasingly requiring that storage temperatures be verified several times per day, and that records be maintained. It is also important to remember the cost associated with losing years of valuable research!

Auditing of this process may be performed by internal QA staff or by external accrediting bodies.  If you want to make life easier – an ‘RAG’ system means less work for your staff, total confidence in the audit information generated and recognition by external bodies of a reliable and professional system.