How does your validation program measure up?
Discover how to evaluate and enhance your validation program with our insightful article. It provides a comprehensive approach to assess....
Resources
Resource center
Subscribe for updates
Featured
Resources
Process ‘discord’: how validation processes change in isolation, and what you can do to prevent it
Without a built-for-purpose validation system in place to standardize validation work processes across a global organization’s manufacturing sites, that process....
25 years of CFR Part 11
Uncover the essentials of FDA's 21 CFR Part 11 regulation for life sciences: its impact on electronic records, compliance, and....
Top 10 validation challenges for life sciences SMBs in 2022
We surveyed medium sized pharmaceutical and biotechnology companies in the United States and Europe to uncover their top ten validation....
3 validation trends to watch in 2022
Each new year brings many new opportunities and challenges for validation and quality professionals across the life sciences sector. 2022....
The environmental impact of validation
What is the environmental impact of validation? At any one time, a large global pharmaceutical company will archive and store....
Data integrity, an increasing regulatory focus
Discover the critical role of data integrity in regulatory compliance through our detailed article. It highlights the intensified regulatory focus....
How paperless validation systems support data integrity
Data Integrity is a major concern for the global pharmaceutical and medical device industries, across many of their business areas.....
Top 5 reasons IT projects fail
Statistics suggest that upwards of 75% of major IT projects fail. They are considered failures because they did not deliver....