Pharmaceutical Industry Articles & Reports - Page 20

An analysis of the Medicare program in 2025, detailing the structure and the significant policy impacts of the One Big Beautiful Bill Act (P.L. 119-21).

Examine 2025 trends for Contract Sales Organizations in pharma. This analysis compares top providers and strategies for HCP engagement and outsourcing.

This article explains how AI tools can validate regulatory dossiers, catch technical errors before submission, and minimize rework for emerging biotech companies.

Examines the evolution of eCTD systems from specialized publishers for regulatory submissions to enterprise platforms that serve as a unified drug lifecycle archive.

This article examines the unique financial challenges facing regional hospitals and details the accounting practices essential for maintaining stability and compliance.

An overview of San Francisco Bay Area neuroscience firms. Examines companies in neurotechnology, BCIs, and neuropharmacology, detailing their focus and status.

An overview of AI in pharmacovigilance, detailing its use in signal detection, case processing automation, and managing regulatory & ethical considerations.

An overview of market access analytics, covering its definition, scope, and role in helping pharmaceutical firms navigate complex payer reimbursement models.

Learn to design, secure, and manage a HIPAA-compliant API. This guide covers HIPAA rules, technical best practices, and risk management for health data.

Examines the use of Veeva CRM across the pharmaceutical and life sciences sectors. Details companies using the platform, with evidence from job postings.

Learn how WORM (Write Once, Read Many) storage ensures data immutability and integrity for electronic records in the highly regulated biotechnology industry.

Examine the technical capabilities of GPT-5, its applications in life sciences and medicine, and the ethical considerations for its use in these fields.

Examines the key scientific journals and trade publications in the pharma and biotech industries, covering peer-review, access models, and target audience.

An educational guide to executing compliant pharmaceutical remarketing. Explores platform policies on Google, Meta, LinkedIn, and Reddit, plus data privacy.

An overview of AI applications in the pharmaceutical sector, from generative AI to ML. Explains key IT management challenges like data, compliance, and security.

Review a list of global online degrees and certificates in AI for pharmaceutical science. Compare programs by level, curriculum, cost, and duration.

An overview of OpenAI's open-weight GPT-OSS models. Examine their technical specifications, benchmark performance, and applications for reasoning in healthcare.

Examines how AI accelerates the pharmaceutical drug pipeline, reducing time to market. Learn about its impact on preclinical testing, clinical trials, and manufacturing.

Examines RegTech adoption challenges for emerging biotechs, focusing on cost and scalability. Explains flexible licensing and deferred-value models for compliance.

An explanation of active learning principles and their adaptation for Large Language Models (LLMs) using human-in-the-loop (HITL) feedback for model alignment.

This article examines strategies for integrating content management systems like Box and Veeva Vault to overcome information silos in regulated environments.

An overview of the pharmaceutical industry's history, from 19th-century origins to the current global market size, sales figures, and regional distribution.

An explanation of regulatory requirements for audit trails under 21 CFR Part 11 and EU Annex 11, covering automation strategies and data integrity measures.

An explanation of the Model Context Protocol (MCP) and its integration with Claude Code. Learn how MCP servers enable AI agents to perform internet searches.