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!

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 front liners whose activities play a vital role in supporting patient outcomes, pharmaceutical manufacturers need to get it right the first time. Recreating activities and reproducing products require extra time, cost, and effort and can leave the company prone to quality risks.The concept of Right First Time originates from the implementation of Six Sigma, […]

The Biggest Trends in Pharmaceutical Manufacturing The pharmaceutical industry has undergone several changes which are often introduced and enforced by regulatory bodies. These changes, which we can also call a revolution, make up Pharma 4.0. Earlier in the day, pharmaceutical operations were manual and required solely the use of paper.However, as technology improved, pharmaceutical manufacturing […]

The Pitfalls of Paper Forms in Pharmaceutical Manufacturing Paper documentation and wet signatures are still all too common in manufacturing operations. At this point, the pitfalls of paper forms outweigh their benefits. This is why many pharmaceutical companies are turning to digital solutions to streamline their processes, reduce paperwork, and make their operations more efficient.With […]

Electronic Forms for Work Instructions and Data Collection Paper-based data collection method has helped companies immensely. Sadly, it cannot keep up with the technological advancement pace, so it has to be substituted with electronic forms.Let’s discuss how electronic forms are changing the industry and the benefits of using electronic forms for work instructions, workflows, and […]

Why Switch to Electronic Room Cleaning? Maintaining a clean manufacturing environment is essential in pharma. The efficacy and compliance of your products and processes relies on accuracy and precision at every step of the manufacturing journey. And that starts with cleaning validation.If clean rooms, surfaces, equipment or packaging is not cleaned thoroughly, entire batches can […]

Corrective and Preventive Action in Pharmaceutical Industry OpsTrakker is built on the latest industry 4.0 trends to be a lightweight and low-overhead solution for GMP operations. Opposed to traditional GMP applications, OpsTrakker focuses on providing high value manufacturing functionality for specific use cases through it’s suite of apps. While traditional systems do a great job […]