Pharma’s reliance on long-form documents and manual versioning cannot keep pace with global complexity. Read More
Author Archives: Santosh Shevade
AI-Powered Translation and Localization in Pharma Content Operations
AI-powered translation—guided by structured content and domain expertise, offers a practical and sustainable path forward. Read More
How AI in Clinical Data Analysis Is Shaping Scientific Narratives
How AI in clinical data analysis helps pharma teams transform trial data into clear, compliant, and compelling scientific narratives. Read More
How Data & AI are Making HCP Engagement Shockingly Personal
With Straive, personalization becomes more than a tech upgrade—it’s a cultural shift that builds stronger, more relevant HCP relationships. Read More
Why RWE Data Curation Needs a Domain-Led Approach
The actual value of RWE lies not just in the breadth of real-world data but also in its ability to curate it with precision, compliance, and contextual understanding. Read More
Breaking Down Data Silos: A Pathway to Enhanced Clinical Insights in Pharma
Straive helps break down pharma data silos for operational agility and better trial and regulatory outcomes. Straive enables this with advanced AI, governance, and integration solutions that unify data across the pharma value chain. Read More
Build vs. Buy in Pharma AI: Why Strategic Partnerships Surpass In-House Builds
Imagine a leading pharmaceutical team, eager to harness AI for drug discovery. Months are spent building an in-house solution, yet six months later, the pilot struggles to deliver results. Read More
The New Intelligence Layer: AI’s Expanding Role in Pharma Content Operations
The real transformation comes from augmentation, not replacement. AI drafts, analyzes, and optimizes, while human experts infuse therapeutic context, validate accuracy, and ensure compliance with medical, legal, and regulatory standards. Read More
AI Meets Domain Expertise: How Straive Builds Pharma Publishing Pipelines That Scale
The demand for faster, high-quality publications in pharma is only increasing. Clinical trial sponsors, medical affairs teams, and regulatory writers all face tight timelines—from first patient in (FPI) to marketing authorization. Read More
Can AI Deliver Automation in Drug Labeling & Compliance?
Organizations can implement real-time compliance checks by embedding AI into the document lifecycle. These systems detect misalignments with regulatory standards before submission, dramatically reducing the need for rework and minimizing audit flags. Read More