With 27 years and billions of uninterrupted doses behind our name, Ritedose 503B Outsourcing delivers on-demand, pre-filled syringe products ready for use in hospitals across the U.S. These ready-to-administer injections can save time in the pharmacy, increase compliance and help clinicians provide safe patient care by reducing potential bedside errors. And with extended dating up to twelve months, you can be assured of having our products readily available.
That means you can get back to meeting your hospital’s patient care needs, without the headache of compounding on the fly.
We deliver sterile, single-dose syringe products necessary for in-hospital care and that meet critical national drug shortages. A 27-year leader in cGMP drug manufacturing, Ritedose uses aseptic production to guarantee sterility and standardized concentrations in every dose.
Innovative packaging allows for extended dating up to 12 months and room temperature storage. Our pre-filled syringes are already diluted, labeled with appropriate cautionary statements, color-coded to ASTM drug class standards, and ready to be administered within OR and acute care settings. Since we offer multiple concentrations and fill volumes for most medications, clinicians have a choice in what they prescribe. It simply couldn’t be more streamlined.
We got it right because we listened. Our products were designed with input from clinical pharmacists and other healthcare professionals to meet your exact needs, enabling you to deliver the highest level of patient care every day. From product packaging and labeling to a robust customer portal for online ordering and trend reports – our entire 503B outsourcing solution was built around you.
Our team of clinical pharmacists and healthcare specialists can help you navigate how ready-to-use products could expand your capacity. Contact us for a virtual audit of your pharmacy resources.
Leave your worries about compliance, contamination and compounding errors to us. Our state-of-the-art 503B facility, connected to our larger manufacturing and packaging facilities, is set up to exceed FDA standards. Meeting the most stringent cGMP and USP 797 guidelines, our highly automated production systems — with robotic filling, material handling and packaging — mitigate errors and provide an aseptic environment. And with manufacturing all under one roof, our quality control is unparalleled.