Pharmaceutical Industry Articles & Reports - Page 23

This article compares the user interfaces of leading conversational AI tools like ChatGPT, Gemini, and Claude, detailing their design, features, and professional impact for business users.

Learn about 21 CFR Part 11, the FDA regulation for electronic records and signatures. This article covers its history, purpose, and significance in the pharmaceutical industry.

Explore Good Manufacturing Practice (GMP) in pharma. Learn its principles, global regulations, implementation, and compliance challenges for quality assurance.

This guide explains GAMP 5, its principles, and lifecycle for computerized system validation in pharma, covering regulatory compliance and real-world applications.

Learn what Computer System Validation (CSV) is, its crucial role in pharmaceutical and biotech compliance, ensuring data integrity and regulatory adherence for patient safety.

Compares leading AI OCR models and tools for PDF to structured text conversion. Examines open-source and commercial solutions, assessing capabilities, accuracy, and use cases.

This report details deploying LLMs on 24GB GPUs, covering model architectures, VRAM needs, and optimization methods for efficient local operation.

Learn about meta-prompting, an advanced technique using LLMs to generate, modify, and optimize their own prompts, enabling iterative and complex task execution.

Explore profiles of top global pharmaceutical thought leaders, including their backgrounds, speaking topics, notable engagements, and industry influence.

Learn to build a pharmaceutical manufacturing plant from concept through commissioning. This guide covers planning, regulatory compliance, design, equipment, quality, validation, and approval.

Explore how AI-powered computer vision is transforming pharmaceutical quality control. Review top vendors, applications, and trends in pharma QC automation.

How AI leaders like Amodei, Hassabis, and Huang are accelerating drug discovery, genomics, and life science breakthroughs—compressing decades into years.

Comprehensive guide to BI and dashboard tools for pharma: Power BI, Tableau, Qlik, Looker, Domo, compliance, pricing, and adoption in life sciences.

How Veeva Crossix and big data are transforming pharma marketing analytics: capabilities, compliance, case studies, and adoption trends in the U.S.

Guide to MarTech API integrations for pharma: CRM, marketing automation, analytics, consent, compliance, and best practices for unified digital engagement.

In-depth guide to U.S. pharmaceutical marketing regulations: FDA, FTC, Sunshine Act, anti-kickback, compliance, and IT obligations for pharma companies.

A practical guide to clinical trial phases 1–3 for pharma IT: objectives, compliance, costs, and IT infrastructure for modern drug development.

Guide to outsourcing HCP marketing in pharma: benefits, risks, industry trends, compliance, and how to manage third-party partnerships effectively.

How Veeva Site Connect streamlines sponsor–CRO–site collaboration: features, adoption, compliance, and comparison to Medidata and Oracle Clinical One.

Best practices for pharma teams to secure first meetings with HCPs: outreach tactics, channel comparison, overcoming gatekeepers, and expert tips for success.

A step-by-step career roadmap for pharma IT professionals: from Veeva admin to enterprise architect. Skills, certifications, salary benchmarks, and real-world examples.

Overview of major HCP data providers, U.S. compliance rules, and best practices for pharma IT. Includes vendor comparison, legal requirements, and governance tips.

How biotech and pharma companies use NetSuite for compliance: FDA 21 CFR Part 11, GxP, HIPAA, SOX, audit trails, e-signatures, and reporting best practices.

Evidence-based UX strategies for digital HCP engagement platforms in pharma: trends, challenges, best practices, and compliance for IT teams.