The Burwood Biotech Blog
Expert insights, regulatory updates, and industry trends for biotech and pharmaceutical professionals
Latest Articles
Understanding the 2023 Pharmacovigilance Guidelines Updates
Recent updates to international pharmacovigilance guidelines. Here's what pharmaceutical companies need to know.
Navigating the New FDA Guidelines for AI in Medical Devices
The FDA has released new guidelines for artificial intelligence and machine learning in medical devices. Here's what manufacturers need to know.
EMA's New Pharmacovigilance Requirements: What You Need to Know
The European Medicines Agency has updated its pharmacovigilance requirements. Learn about the key changes and how they affect pharmaceutical companies.
Clinical Trial Design Optimization: Balancing Speed and Quality
Effective clinical trial design is crucial for successful drug development. Learn strategies to optimize your trials for both speed and quality.
Healthcare IT Compliance: Navigating HIPAA and GDPR Requirements
Healthcare IT systems must comply with multiple regulatory frameworks. This article explores strategies for meeting HIPAA and GDPR requirements.