Across the world, Russian ransomware attacks increased in 2021. Ransomware incidents in the US increased 82% from 2019 to 2021, and the US government is closing ranks with energy firms to guard against attacks. How does this affect pharmaceutical and medical device...
News & Blog
The Pitfalls of Data Migration
Did you know that the FDA regulates data integrity? Pharmaceutical and Medical Device industries must operate in accordance with current Good Manufacturing Practices (cGMP) for regulatory industries, such as the FDA and MHRA, to deem a product as safe for consumers....
Paperless Validation – What is it and why you need it
Pharmaceutical and biotechnology companies need to assure product quality using validated equipment and computer systems. Computer Systems Validation (CSV) is the process of ensuring that equipment, software, spreadsheets, utilities, and other computerized processes...
Mastering Stress in the Great Resignation of 2022
In our last blog article on Re-Thinking the Great Resignation of 2022, we highlighted the impact of transformative experiences on decision-making and problem-solving. Another significant element during the COVID-19 pandemic era is the chronic presence of stress and...
Why Electronic Document Routing is the Way to Go
When it comes to routing documents, whether it’s a new document, a revision, or a periodic review of the record, the process can be long and tedious. If your company is still using the printed paper version of routing, it may be time to step into the new world of...
AuditUtopia® vs. ACE Inspection® Management Software
Undergoing inspections and audits is a harrowing experience. Before the FDA, EPA, or other regulatory agency inspectors visit, you need to form an Inspection Team within your company. When the inspector arrives, making a good impression sets a positive tone because...
ACE SuperVision™ for Google Glass Enterprise 2.0
PSC™ has recently taken the software you know and love, ACE™, and integrated it with Google Glass Enterprise! ACE SuperVision™ allows companies like yours to put safety first while streamlining your workflow processes. Together, you will have the same capabilities...
The Importance of Computer Systems Validation
Validation is essential in maintaining the quality of your products and a key requirement for GxP compliance. This is necessary not only for your facility, equipment, products, and processes but also for your computer systems. We focus here on computer systems...
What is the importance of Adverse Event Reporting?
What is an Adverse Event Reporting System (AERS)? The Adverse Event Reporting System (AERS) is a computerized information database designed to support the life sciences, healthcare, biotechnology & FDA agency post-marketing safety surveillance program for all...
What is the Significance of Electronic Document Management Systems in the Life Science Industry?
Accurate record management is a crucial operation for the organizations in Biotechnology, Life sciences, Pharmaceutical and Medical Equipment domains. The document content is growing enormously and manual sorting of the records makes it tedious & prone to errors....