With numerous eTMF software options available in the market, it is essential to know what features to look for when selecting the right solution for your clinical trials.
Top Features in ETMF Software for Clinical Trials Read More »
Learn how seasoned experts evaluate and successfully select CRO Partners
Finding the best CRO partner for your clinical trial Read More »
SureClinical eTMF Passes FDA Inspection Clinical trial systems and processes are advancing at a fast rate. We’ve come a long way from truckloads of paper document files and 3-part NCR case report forms. One thing has not changed quite so dramatically: The FDA Audit. Before a new drug, device or biologic can be reviewed and
FDA Audit of eTMF Trial Master File System Read More »
Trust is the cornerstone of all health and life science interactions, whether it’s following Good Clinical Practice in running clinical trials or in a patient-doctor relationship. The need for high trust carries throughout everything, including how documents and people are validated. I sat down with our CEO, Zack Schmidt, who shared his insights into why
High Trust Signing – How to Ensure your eSigned documents are Compliant Read More »
The pursuit of optimizing the clinical trial process frequently relies on the intense effort to manage the trial project with a clinical trial management system (CTMS) and the thousands of regulatory documents through an electronic trial master file (ETMF). What we’ve seen as an unmet need is how to optimize Investigator Site Files (ISF) management
EISF: The Key to Site Good Clinical Practice Read More »
SureISF is designed to enable clinical sites to collaboratively view, share, digitally esign, comment on and manage site-specific content.
Introducing SureISF Regulatory Cloud Application for Clinical Sites Read More »
