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  Unlocking speed, accuracy, compliance, and innovation in the clinical trial value chain through Enterprise AI solutions Clinical trials are becoming increasingly complex, data-intensive, and regulated. Life sciences organizations must manage massive volumes of structured and unstructured data while maintaining strict compliance and accelerating timelines. In this environment, unlocking speed, accuracy, compliance, and innovation in the clinical trial value chain through Enterprise AI solutions is no longer a competitive advantage—it is a necessity. Enterprise AI enables organizations to modernize clinical trials by embedding intelligence, automation, and governance across the entire value chain. Below are seven powerful ways Enterprise AI is transforming clinical trials . 1. Accelerating Patient Identification and Recruitment Patient recruitment remains one of the biggest causes of clinical trial delays. Manual eligibility screening and fragmented data sources slow down enro...

 As enterprises generate, store, and consume unprecedented volumes of data, data governance has become a business-critical discipline. information governance platform Yet many organizations struggle not because of technology gaps, but because of unclear ownership and accountability . This is where a data governance roles and responsibilities matrix becomes essential. A well-defined matrix clarifies who owns data, who manages it, who protects it, and who ensures compliance —turning governance from theory into execution. In this guide, we break down: What a data governance roles and responsibilities matrix is Why it matters for large enterprises Key governance roles and responsibilities A practical matrix you can adapt Best practices for implementation How enterprise platforms like Solix enable governance at scale What Is a Data Governance Roles and Responsibilities Matrix? A data governance roles and responsibilities matrix is a structured framework—oft...

  As life sciences companies expand their digital ecosystems, the pressure to maintain FDA 21 CFR Part 11 and GxP Compliance continues to rise. The regulatory landscape is no longer limited to simple document control and audit trails. Today, organizations must manage massive data flows from cloud systems, electronic records, AI-driven workflows, automated labs, and global clinical operations. Without a scalable compliance framework, even small gaps can lead to audit failures, fines, product delays, or reputational damage. This article explains how enterprises can build a future-ready, scalable, and technology-driven compliance foundation designed for modern data complexity. Why Scalability Matters in FDA 21 CFR Part 11 and GxP Compliance Traditional compliance systems were built to manage structured records inside isolated applications. But today’s environment includes: Distributed cloud platforms AI/ML pipelines Cross-site manufacturing Global supply chains Hybr...

 Global regulatory reforms are moving faster than most enterprise IT teams can adapt. New data protection laws, digital governance frameworks, and industry-specific mandates are rewriting what organizations must store, how long they must store it, and how quickly they must retrieve it during audits. This changing landscape has triggered a compliance archiving revolution   one where legacy storage systems and outdated archiving practices simply cannot keep up. To stay compliant, audit-ready, and operationally efficient, enterprises are shifting toward modern, intelligence-driven archiving systems. Here's how regulatory reforms are reshaping the archiving playbook — and why forward-looking organizations are embracing platforms like Solix to meet these escalating demands.   When Compliance Becomes the Catalyst 1. Compliance Is No Longer a Back-Office Function — It’s a Strategic Priority A decade ago, compliance was seen as a legal or administrative requirement. Tod...

 Email remains the backbone of enterprise communication. Despite the rise of collaboration apps and messaging platforms, email continues to hold the most critical conversations, contractual exchanges, approvals, customer interactions, and internal decision-making trails. Over time, this makes email not just a communication tool—but one of the most valuable (and risky) data assets an organization owns. Yet most companies still treat email retention casually. Employees store messages for years, delete important emails without guidance, or hold large volumes of unstructured messages indefinitely. Without a structured, enforced retention policy, email becomes a chaotic repository full of legal, compliance, and security risks.  What are the Benefits of Email Archiving A well-designed email data retention policy is not just a best practice—it is a legal and operational necessity. Here’s why every modern enterprise must take it seriously. What Is an Email Retention Policy? An em...