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 […]

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 […]

Electronic logbooks, eLogBooks, or e-logs in the pharmaceutical industry aren’t exactly new. Many manufacturers have been using software for years to track equipment, production, and manufacturing of raw materials and finished goods. eLogBooks reduce paper use by eliminating paper documents, improving visibility into production processes, automating data collection with manual data entry, implementing risk management […]

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, […]

Agility in New Areas of Life Sciences and Pharmaceutical Manufacturing Pharmaceutical manufacturing has traditionally relied on centralized facilities for mass pharmaceutical production and distribution. As good as this method is, it may be limited when looking at the larger industry trends. This method guarantees product quality and consistency, but its rigidity prevents new manufacturing methods […]

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 […]

Common Compliance Mistakes That Can Get You in Trouble with the FDA Specific laws guide companies in every sector. Compliance with those laws aids effective manufacturing and keeps customers safe, especially in the pharmaceutical and biotechnology industries.Since these industries focus on human health and patient outcomes, adherence to health and safety regulations is crucial. Therefore, […]

Corrective and Preventive Action in Pharmaceutical Industry Getting it right the first time in the pharmaceutical industry is an absolute priority. If that seems obvious, it’s because it is. More so than in other industries, small errors have the potential to cause enormous problems down the line. This is true of large and complex scientific miscalculations, and […]

¡Vamo a Darle! EIS PR is Open for Business! Today, EIS Inc. announced the opening of Enhanced Information Solutions Limited Puerto Rico Liaison Office. EIS Puerto Rico is a 100% owned subsidiary of EIS Inc. and is established as part of EIS’s strategic objectives and client focus to provide high quality consulting and manufacturing system […]

How Going Paperless Can Reduce Your Carbon Footprint It’s never been more important to reduce our impact on the environment. Environmental and organizational pressure to reduce our carbon footprint is increasing. One way to reduce your business’s footprint is by joining the paperless revolution. Fortunately, reducing your carbon footprint does not have to be such a […]