
Learn how to choose eCTD software for small pharma. This guide covers regulatory compliance, global submission timelines for FDA & EMA, and eCTD v4.0 updates.

Learn how to choose eCTD software for small pharma. This guide covers regulatory compliance, global submission timelines for FDA & EMA, and eCTD v4.0 updates.

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 Lorenz docuBridge, a key eCTD publishing software for biotech. This guide covers its features, editions, and use by regulators for regulatory submis

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

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.

A comprehensive guide to building and scaling Veeva Vault and CRM data pipelines for terabyte-scale datasets in the pharmaceutical industry, with a focus on compliance and performance.

An in-depth analysis of the biotech ecosystem in the San Francisco Bay Area, examining key players, emerging startups, investment trends, and innovation clusters as of January 2026. Updated with latest data on 23andMe bankruptcy, major acquisitions, and 2025 layoffs.

Explore how MCP is revolutionizing data integration and AI applications in pharmaceutical research, clinical trials, and healthcare systems for enhanced compliance.

A comprehensive overview of Customer Relationship Management (CRM) platforms tailored for biotech companies, comparing various solutions and their features for compliance, sales, and customer relationship management in the life sciences sector.