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Fact Sheet: Blur™: Simplifying and Streamlining Clinical Trial Transparency Compliance

Fact Sheet: Blur™: Simplifying and Streamlining Clinical Trial Transparency Compliance

by Instem Team | Jun 30, 2025 | Resources

Industry-Leading Clinical Trial Transparency Platform for Compliant Data and Document De-Identification and Risk Measurement. Built in collaboration with top pharmaceutical sponsors, Blur is the number one Clinical Trial Transparency (CTT) platform. Maximize your data...
Introducing Blur™ 2.9: Smarter, Faster Anonymization for Clinical Trial Transparency

Introducing Blur™ 2.9: Smarter, Faster Anonymization for Clinical Trial Transparency

by Instem Team | Jun 27, 2025 | Clinical, Press Releases

As regulatory expectations evolve and the demand for secure, reusable clinical trial data grows, life sciences teams need more than just a basic anonymization tool. What they really need is a clinical trial transparency platform that’s scalable, intelligent, and built...
Case Study: Hydrating a Data Lake with Clinical Trial Data: Automating Data De-Identification for Secondary Use

Case Study: Hydrating a Data Lake with Clinical Trial Data: Automating Data De-Identification for Secondary Use

by Instem Team | Jun 24, 2025 | Resources

A top pharmaceutical sponsor had 84 clinical trials worth of data they wanted to utilize to its full potential to research new therapies. However, due to regulations, patient data can only be used for what it was initially collected. On top of that, the data sets were...
Driving Pathology Forward: Instem Strengthens Provantis® with Continued Investment and Innovation

Driving Pathology Forward: Instem Strengthens Provantis® with Continued Investment and Innovation

by Instem Team | Jun 23, 2025 | Press Releases, Provantis, Study Management

BOSTON – June 23, 2025 – Instem, a global leader in life sciences software solutions, today announced significant enhancements to its Provantis Pathology module, a cornerstone of the company’s industry-leading platform for preclinical study management. These latest...
Whitepaper: Preparing Pharma and CROs for Audits by the FDA

Whitepaper: Preparing Pharma and CROs for Audits by the FDA

by Instem Team | Jun 20, 2025 | Resources

Clinical research organizations and pharmaceutical sponsors often face significant delays and operational strain due to the complexity of computer system validation (CSV). Traditional validation processes can consume valuable IT and QA resources, slow deployment...
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