Merging the most critical components of anesthesia — medication delivery and clinical information — to maximize quality of care and return on investment.

The DocuSys solution originated in 1981 when Dr. Robert Evans, then a resident in Anesthesiology, experienced a medication error. The ease with which this adverse drug event (ADE) occurred prompted him to develop a breakthrough system that could warn the anesthesia provider in advance of administering a drug contraindicated by allergy, medical condition or physiologic status.

Today, DocuSys technologies include the most complete anesthesia information management system (AIMS) in the industry and the first medication management system for anesthesia. The complementary technologies work in unison and follow the natural progression of a patient throughout the PeriOperative continuum.

The company has received 510(k) clearance from the Food and Drug Administration (FDA) to market its technology and is a registered medical device manufacturer in accordance with FDA guidelines. This FDA designation validates DocuSys’ capabilities of providing the market with products that have undergone a rigorous quality assurance process and furthers the patient safety objectives of healthcare providers.



DocuSys Firsts in the Industry

• First to digitize bolus syringe medication administration
• First bar coding system for operating room medications
• First medication error prevention support system for the operating room
• First to create a closed-loop electronic narcotic tracking system
• First AIMS to utilize Microsoft.NET platform
• First to integrate an AIMS with a medication dispensing cabinet