Webinar April 4th, 2023 - In 2022 Enhanced Information Solutions released eDatasheet for Manually entering data into PI. At AVEVA World, we introduced EF Manager for Manually creating and editing PI Event Frames. EIS is hosting a Webinar on Manually Entering data into PI with eDatasheet and manually creating and editing PI Event Frames with EF Manager.

PI Event Frame Management and Electronic Workflows October 26, 2022 Online Experience Hosted by EIS PI Event Frames are a powerful tool to analyze batches and alarms.  One of the challenges is how to manually create PI Event Frames and intuitively edit Event Frames without giving PI System Explorer to non-PI System Administrators.  Additionally, many […]

eDatasheet: Manual Entry to a PI Data Historian Manual data entry into a PI system typically involves cumbersome and complex solutions. Various industries, including the life sciences, power & utilities, aviation, and more all require the ability for manual entry to a data historian. While mature data historization strategies are in place, they often fail to […]

Join us for the annual AVEVA World Conference in San Francisco! EIS has deep experience in implementing and supporting the AVEVA (OSIsoft) PI System, across a variety of industries. Visit us at Booth #56 to learn more about our PI Services and Solutions, including eDatasheet - Manual Data Entry and Logging to a PI System.

21 CFR Part 11: A Brief Overview of cGMP Manufacturing companies in the life sciences must follow FDA 21 CFR 11 and EU GMP Annex 11 requirements in order to sell products in the US and EU. As many organizations across the industry scale up production from clinical to commercial operations, adequate documentation and access […]

Thank you for joining us at Pharma MES Berlin 2022! Get in touch to learn more about OpsTrakker eLogBooks, eForms, and our digital solutions!

Good manufacturing practice (GMP) is a set of guidelines that manufacturers must follow to ensure that their products are safe, compliant, and high-quality. The FDA lays down these guidelines to provide a thorough and unadulterated process of product manufacture. GMP focuses on processes and procedures to reduce the risk of introducing contaminants or non-approved substances […]

The pharmaceutical industry is one of the world’s most massive, intricate, and beneficial industries today. It creates new developments which might be challenging to track in some cases. Despite this, the impact of these pharmaceutical innovations and manufacturing solutions is immeasurable as they sustain numerous lives.This brings us to discuss the pharmaceutical industry and drug […]

Process development is the process of creating new and improved production methods. It aims to optimize solutions to meet customer needs, maintain regulatory compliance, reduce costs and improve product quality. Process development in the pharmaceutical industry is a collaborative effort between operators, engineers, technicians, marketers, and production specialists. It involves designing processes, testing different scenarios, […]

As the pharmaceutical industry continues to experience a great wave of growth, it is hard not to mention advanced manufacturing. As a result, advanced manufacturing has become a buzzword often used when discussing the future of factories, including pharmaceutical manufacturing. Combining its various elements aids effective pharma production while it brings flexibility. So stay glued […]