Resources

This white paper explores the evolving regulatory landscape and the delicate balance between protecting patient privacy and maximizing data utility.

This whitepaper discusses modern problems that Clinical Trial Transparency teams face when trying to balance patient privacy, data utility, and manage risk while in an evolving regulatory landscape.

A leading European pharmaceutical company enhances efficiency, compliance, and data integrity with Instem’s Cyto Study Manager™.

Cyto Study Manager™ supports diverse in vivo and in vitro assays, maintains GLP and 21 CFR Part 11 compliance, and generates complete, auditable data for regulatory submission.

Built by Pharma for Pharma, Blur is the Best-In-Class SaaS Solution for De-Identification of Clinical Trial Data, Safeguarding Patient Privacy, and Ensuring Regulatory Compliance.

Complete the form to read the case study about how one global pharmaceutical sponsor was able to anonymize 84 clinical trials’ worth of data in different formats in only 30 minutes.

This whitepaper explores how turnkey validation solutions are helping CROs and pharmaceutical companies streamline compliance, reduce risk, and accelerate clinical operations.

BioRails® supports both structured experimentation and the integration of unstructured results into a structured environment.

This white paper explores the principles of master data management and explains how BioRails® implements flexible, scalable strategies to support evolving organizational needs without the burden of replication or fragile integrations.