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Jan 9, 2024
CSV Vs CSA – Unpacking FDA’s Revised Software Validation
Embrace cutting-edge innovation in Quality Assurance (QA) through a comprehensive understa...
Read moreWriting
Mar 15, 2023
Grant Writing For Regulatory Processes – White Paper
Grant writing is preparing and submitting proposals to secure funding from grant-making organizati...
Read moreDec 5, 2022
The 5 Most Common Data Migration Pitfalls
A Data migration is a daunting, but necessary task when companies undergo digital transformati...
Read moreOct 11, 2022
How to Ace Your Inspections: Keys to Inspection Readiness
On-site and Remote Inspection Management Regulatory inspections can be some of the most int...
Read moreMar 12, 2022
Use of Multi-Disciplinary Validation Teams for GXP Projects White Paper
Maximize efficiency and effectiveness in your validation projects by utilizing multi-disciplinary ...
Read moreComputerized Systems
White Paper
Mar 10, 2022
Paperless Validation – What is it and why you need it
Pharmaceutical and biotechnology companies need to assure product quality using validated equipmen...
Read moreFeb 3, 2022
Applications for Quality Risk Management in Facility Operations
This is the final installment in PSC Biotech®’s series on Quality Risk Management (QRM) in Comm...
Read moreJan 20, 2022
Microbial Contamination Control White Paper
Microbial contamination control encompasses many areas in the manufacturing process. You can contr...
Read moreProject Management
White Paper
Jan 20, 2022
Environmental Monitoring, Keeping Your Rooms Ready
What is environmental monitoring? Environmental monitoring describes the systems that allow...
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