Pharmaceutical Industry Articles & Reports - Page 18

Learn how to create apps for ChatGPT in 2025. This guide explains the OpenAI Apps SDK, the GPT Store, custom GPTs, and provides a step-by-step developer workflo

This article profiles five leading technology companies in healthcare AI. It examines their key solutions for data analytics, patient engagement, and life scien

Learn best practices to evaluate CRO costs for your clinical trial budget. This guide covers RFPs, comparing pricing models, and analyzing CRO proposal details.

A detailed overview of IQVIA's technology solutions for life sciences. Learn about platforms for data management, commercial engagement, analytics, and RWE.

Learn how to build robust LLM evaluation frameworks for biotech. This guide covers key metrics, biomedical benchmarks (BLUE, BLURB), and methods for ensuring ac

An overview of Next Best Action (NBA) in pharma. Learn how this AI strategy uses data to suggest optimal engagement actions for healthcare professionals.

An analysis of China's open-source LLM landscape in 2025. Covers key models like Qwen, Ernie, and GLM from major tech firms and leading AI startups.

Learn the hardware requirements for running OpenAI's GPT-OSS-20B model locally. This guide covers GPU VRAM, CPU, system RAM, and other key components.

An examination of the five key technical innovations behind ChatGPT, from the Transformer architecture and pretraining to RLHF, hardware, and tokenization.

An analysis of leading software for molecular modeling and simulation. Learn about features, theoretical methods (MD, QM), performance, and use cases.

Learn about Apache Airflow's core architecture, including DAGs, schedulers, and executors, and its application for building data workflows in life sciences.

An in-depth technical comparison of five cheminformatics platforms, evaluating features like SAR/QSAR, ADMET prediction, and chemical library management.

Examines the 2025 AI regulatory frameworks for biopharma in the U.S., EU, U.K., and Canada. Details compliance obligations for GenAI, GxP, and SaMD.

Learn the architectural differences between event sourcing and queue-based systems. This article covers immutable event logs, data traceability, and replayability.

Learn about Mixture of Experts (MoE) models, a neural network architecture using specialized experts and a gating mechanism to efficiently scale computation.

An educational overview of hospice EMR systems, including essential features for documentation, scheduling, billing, and ensuring HIPAA compliance.

An overview of GAMP 5 guidelines for validating computerized systems. Explains the risk-based approach, system lifecycle, and updates for AI and cloud tech.

Learn about the specialized software tools used across the drug development lifecycle, from discovery and preclinical research to manufacturing and commercialization.

An analysis of Regulatory Information Management (RIM) systems, covering their role in life science compliance, eCTD submissions, and enterprise integration.

This article provides a technical overview of pharmacovigilance software, detailing core functions, regulatory compliance, and a comparison of leading platforms.

Learn what Policy as Code (PaC) is and why it is used in healthcare to automate enforcement of security, privacy, and compliance regulations.

Examines how to apply Git version control workflows to satisfy FDA compliance, covering traceability, audit trails, and standards like 21 CFR Part 11 & IEC 62304.

Learn about FHIR (Fast Healthcare Interoperability Resources), the modern HL7 standard for exchanging health data using web APIs and self-contained resources.

An overview of AI agents in pharmacovigilance (PV), detailing their application in processing safety data and managing the increasing volume of ICSRs.