The Complete Guide To Correspondence Management In Life Sciences
Last Updated: September 2026
What is correspondence management in life sciences, and how should regulated teams track it?
Correspondence management means treating regulatory, clinical, and...
Regulatory Document Management Systems Explained
SOP drift. Duplicate files. Missed periodic reviews. Failed audits. These are all symptoms of a document management process that isn't built for regulatory rigor.
A Helpful Guide To The Regulatory Submission Process
Last Updated: September 2026
What does the regulatory submission process actually involve, from pre-submission planning through eCTD publishing and post-approval upkeep?
A regulatory...
21 CFR Part 11 Compliance Checklist
Last Updated: September 2026
What does a 21 CFR Part 11 compliance checklist need to cover?
21 CFR Part 11 governs how the FDA treats electronic records and signatures for regulated life...
All About 21 CFR Part 11 Compliance
What is 21 CFR Part 11?
21 CFR Part 11 is a regulation established by the U.S. Food and Drug Administration (FDA) that sets the criteria for electronic records and electronic signatures...
RIM Explained: Regulatory Information Management & Systems
Last Updated: August 2026
What is a RIM system, and how does it support global regulatory submissions planning?
A RIM (Regulatory Information Management) system centralizes regulatory data,...
EU MDR vs. FDA Regulations: Key Differences
Introduction to Regulations
Medical device manufacturers operating in both the European Union and the United States must comply with two distinct regulatory frameworks: the European Union...
How to Track Regulatory Correspondence in Kivo
Tracking agency commitments is essential for obvious reasons, but can be stressful without a system or process to manage them. With Kivo'sCorrespondence Tracking,you'll never have to...
How to Review and Approved Controlled Documents in Kivo
Document authoring is one of the most essential activities in Regulatory, Clinical, and Quality operations. Regulations such as CFR Part 11 requiring compliant e-Signatures dictate the way...
How to Manage Projects Efficiently with Automated Reporting
One of the more challenging aspects of clinical trial management is visibility. The sheer number of outsourced partners - sites, CROs, writers, consultants, vendors, etc - who often have...