Pharmaceutical Industry Articles & Reports - Page 12

Learn about the ANSI X12 EDI protocol. This guide explains the structure of X12 transaction sets, with a deep dive into healthcare's 270/271 and 278 transaction

Explore the 2024 Veeva application support provider landscape. This analysis covers key players, market size, and managed services for Veeva Vault and CRM.

Learn why over 85% of clinical trials face delays. This analysis covers the key scientific, operational, and regulatory challenges that slow drug progression.

Learn the complete history of GLP-1 drugs. Explore the incretin effect, the discovery of exenatide, and their evolution from diabetes to obesity treatment.

An in-depth guide to US drug formularies, pharmacy benefits, and prior authorization (PA). Learn how P&T committees, tiers, and ePA systems work to manage costs

Get a complete list of Real-Time Benefits Check (RTBC) modules and providers. Learn how solutions from Surescripts, DrFirst, & RxRevu work within the EHR.

Learn what a health insurance formulary is. This guide explains the drug list, tiers, and cost-sharing used by PBMs to control prescription costs and access.

Learn about Veeva Basics, a pre-configured suite of GxP software for emerging biotechs. This guide analyzes its features, modules, and implementation model.

Learn about the Veeva Vault CRM migration from Salesforce. This roadmap covers the official timeline, technical steps, data migration best practices, and key ch

An evidence-based analysis of the top 5 electronic prior authorization (ePA) platforms. Compare systems like CoverMyMeds & Surescripts and their impact on workf

Learn about the NCPDP SCRIPT standard, the U.S. foundation for electronic prescribing (e-prescribing). This guide covers key versions, transactions, and CMS man

A technical analysis of cost-effective LLMs. Compare API pricing, performance benchmarks, and features for Gemini Flash, Claude Haiku, GPT-5 Mini, and more.

Learn the 9 ALCOA+ principles for GxP data integrity. This complete guide explains each attribute, FDA & EMA regulations, and compliance for pharma and life sci

Explore Veeva QualityOne, the unified cloud QMS for regulated industries like CPG & chemicals. This guide explains its key features, modules, and role in digita

A complete LLM API pricing comparison for 2025. Analyze token-based costs for OpenAI (GPT-5), Google Gemini, Anthropic Claude, Grok, and DeepSeek models.

An educational analysis of AI biotech funding in 2025. Explore venture capital investment trends, funding data, and key deals in AI for drug discovery.

Explore the key drivers behind major pharma and CRO layoffs in 2025-2026. This analysis covers economic pressures, patent cliffs, and R&D shifts at top companie

Analysis of AI medical devices in 2025. Learn about market growth, 950+ FDA-cleared devices, new regulations like the EU AI Act, and key clinical challenges.

Learn why automating Veeva Vault metadata change detection is vital for life sciences compliance. This guide covers methods to prevent data risks and ensure aud

Learn what an electronic Investigator Site File (eISF) is and its role in clinical trials. This guide explains eISF vs. eTMF, regulatory compliance, and benefit

An educational guide to Regulatory Information Management (RIM) systems and their role in adopting ISO IDMP standards for life sciences compliance and data inte

Learn about the TMF Reference Model, the industry-standard taxonomy for organizing Trial Master File (TMF) documents in clinical trials for ICH-GCP compliance.

A guide to finding drugs in the clinical pipeline (Phase I-III). Learn to use key resources like ClinicalTrials.gov, regulatory databases, and commercial tracke

Learn about Veeva SiteVault, a free eISF solution for clinical research sites. This guide analyzes its features, compliance (21 CFR Part 11), and impact on site