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We are very proud that we provide Scilife's Platform as a pre-validated software. This lifts 95% of the validation burden off the shoulders of our customers. This being said, we often receive a question about the remaining 5% of the part. T...

Tech innovations are driving the rapid evolution of everything humans do, and auditing is no exception. Since 2020, remote or virtual audits have become commonplace, born out of necessity in a time when on-site audits were simply impossible. Due to t...

A well-trained and reliable workforce is fundamental. It’s the lifeblood that drives any process to run smoothly, especially in GMP (Good Manufacturing Practices). In the life sciences industry, potentially life-saving knowledge and critical complian...

Old habits die hard and a paper-based QMS system is that old habit that has more disadvantages than advantages. Whereas the new eQMS system holds the seeds for success in future regulatory audits. That is why the bad old habit of using a paper-based ...

In GxP compliance environments, the importance of having a well-trained and reliable workforce cannot be overestimated. In the life sciences sector, where life-saving knowledge and compliance procedures are continually being developed and must be con...

We are very proud that we provide Scilife's Platform as a pre-validated software. This lifts 95% of the validation burden off the shoulders of our customers. This being said, we often receive a question about the remaining 5% of the part. Therefore i...

Stacks of paper, what a hassle!  Staying on top of who printed what, where, and when is a common struggle for many life science companies. Document reconciliation is even more of a challenge. Printing may be unavoidable, but staying compliant and kee...