With an exclusive focus on life science manufacturing, our platform and services were built for pharma. Don’t waste time and effort trying to adapt a system built for the factory to the needs of your facility.
Augmented Work Instructions (AWI) is the only cloud-native, digital work instructions software that:
Whether you’re on paper or on a digital system, we can help you take the first step on your journey to Pharma 4.0.
Developed for life science teams, AWI’s intuitive, no-code configuration enables procedure creation with formula calculations and advanced capabilities like linked procedures, parallel execution, branching, and enforcement logic — without reliance on a third-party.
Build new digital instructions in hours with procedure templates, or transform an existing paper-based procedure into an editable digital process. Save hours with a design tool that converts a PDF into modifiable digital steps.
Make operating instructions crystal clear by enhancing any step of a procedure with technique media: photo, video, and AR overlays.
Author recipes together in real time across your organization, including CDMOs, and experts with our integrated virtual collaboration and word processing tools. Maintain audit trails with the platform’s 21 CFR Part 11 compliance and SOC2 and ISO certifications.
AWI’s cloud-native mobile app and hands-free, voice-enabled headset move to where you are working. Our cleanable, ATEX-certified headsets are perfectly suited to PPE, and are optimized for use in all environments — the suite, cleanrooms, and more.
Make right first-time execution the standard with non-conformance alerts and programmable guardrails that prevent operators from incorrectly completing a step when values diverge from defined ranges.
Execute together or assign individual steps to different users while providing updates and real-time visibility into the process.
Keep pace with your operations by establishing parameters that can change depending on stage — pre-clinical to commercial — or quantity to easily scale up or down.
Save 10-12 weeks of validation effort by using a platform that has been independently verified to meet stringent pharma regulations like the FDA’s Current Good Manufacturing Practices (CGMPs) requirements. Establish audit trails with the platform’s 21 CFR Part 11 compliance and SOC2 and ISO certifications.
Use exception review to identify events that may have an impact before they slow the whole manufacturing process. Track the execution of a workflow in real time to monitor progress and manufacture at a greater speed.
Reduce paper-based legwork that leads to delays in product release and GMP compliance with digitally documented steps and built-in data integrity checks.
Improve data traceability by routing to the right sources and retaining all past and future documentation on the cloud. Digital work instructions and associated documentation allow for end-to-end lifecycle visibility.
Manufacturing Execution System (MES)
Continue your journey to Pharma 4.0 by evolving from digital work instructions to full MES capabilities with the Tempo MES when your organization is ready. Don’t piece together apps on a developer platform when you can grow with a platform built for pharma.
Laboratory Execution System (LES)
Collaborate easily and efficiently with a quality control system designed for the modern scientist. With intuitive digital instructions, you can empower your scientists to execute test methods and manage samples, materials, and instruments at scale and hands-free.
Tempo Manufacturing Cloud
With a composable system, teams across your enterprise can use the right level of functionality to meet their current maturity needs. As teams get more sophisticated, they can seamlessly add on additional capabilities without coding or data transfer.
Tie your system together with collaboration software and devices that are purpose-built to comply with pharma regulations. Tandem allows you to work as one team from anywhere.