ATLANTA–(BUSINESS WIRE)–Portal Innovations announced continued growth at Portal Atlanta at Science Square, with the addition of seven new member companies, bringing the total ecosystem to 32 biotech, medtech, digital health, and cleantech, organizations served, just 15 months after launch. The milestone – which includes 7 new members in just the month of January 2026 alone…
Introduction In the complex and highly regulated world of clinical research, medical writing plays a pivotal role in bridging the gap between scientific innovation and regulatory approval. From drafting clinical trial protocols to preparing submissions for regulatory authorities, medical writers ensure that scientific data is communicated clearly, accurately, and compliantly. Their expertise not only accelerates…
Clinical Data Management (CDM) is a critical component of clinical research, ensuring that data collected during trials is accurate, reliable, and compliant with regulatory standards. However, various challenges can lead to data inconsistencies, errors, and regulatory setbacks. This article explores the most common pitfalls in CDM and strategies to mitigate them. 1. Inadequate Data Quality…
