Insights That Move You Forward
Helping you make smarter decisions, avoid costly missteps, & bring safe, effective products to market with confidence
Real-World Impact: Poor Data Integrity Examples from Recent Rejections
Regulatory rejections often stem from preventable data integrity failures—like falsified lab results, poor traceability, or incomplete safety documentation. These errors delay patient access and damage credibility. Learn from real-world examples and see how NMCG helps sponsors safeguard submissions from costly pitfalls.
Common Protocol Pitfalls and How We Help You Avoid Them
Clinical trial protocols often fail when they’re overly complex, misaligned with regulatory expectations, or impractical for sites and study subjects. These pitfalls cause delays, costly amendments, and wasted resources. NMCG helps sponsors avoid common missteps by designing clear, compliant, and right-sized protocols built for success from the start.
How the FDA Prioritizes Cybersecurity in Device Submissions
Cybersecurity is now inseparable from patient safety. The FDA views it as a critical factor in determining whether a medical device is safe and effective for market approval. Learn how the agency prioritizes cybersecurity in submissions—and what steps sponsors must take to avoid delays, protect patients, and build regulator-ready strategies.