FDAMap, a global regulatory and clinical expert firm, is significantly expanding its focus on regenerative medicine in South America. The company is actively collaborating with local healthcare providers and patients to advance access to and the development of safe, non-manipulated stem cell therapies in the region. FDAMap’s core initiative centers on non-manipulated stem cells, primarily … Read more
The Gulf Cooperation Council (GCC) region is actively focusing on developing its healthcare sector, particularly in regenerative medicine using established stem cell approaches. FDAMap, led by the world’s leading authority on regenerative medicine, Dr. Mukesh Kumar, initiated development of stem cell therapies in the region. Regenerative therapies using non-manipulated stem cells, such as Mesenchymal Stem … Read more
For years, randomized clinical trials (RCTs) have been the gold standard for drug approvals, but they often fall short of reflecting real-world clinical practice. Real-World Evidence (RWE), data generated during routine clinical use, is expected to address this deficiency. While the US Food and Drug Administration (FDA) has been actively incorporating RWE, a recent study … Read more
Artificial Intelligence (AI) offers unprecedented tools for diagnosis and treatment. However, a new cross-sectional study of nearly 1,000 FDA-approved AI-enabled medical devices reveals a troubling gap between regulatory approval and robust clinical evidence. Questions are raised about the reliability of these tools to perform safely and effectively for every patient, regardless of their background or … Read more
Imagine dedicating years and millions of dollars to developing a life-changing new medicine, only to have its application refused by the FDA due to a preventable administrative error. This costly setback, the Refuse to File (RTF) action, consumes immense resources and delays promising treatments from reaching patients. The FDA RTF checklists used by its own … Read more
The federal government is in a funding lapse, a formal way of saying Congress didn’t pass a budget, and the government has “shut down.” If you’re a company developing a new medicine or device, you might assume the FDA’s doors are completely closed—but that is a critical misconception. While a shutdown does create significant regulatory … Read more
A key question for the developers of biosimilars is the studies needed to support interchangeability with the reference biologic. A new FDA Guidance Document, released this week, provides the current rationale for the need for a Comparative Efficacy Study (CES). This draft guidance describes updated scientific considerations regarding a comparative clinical study with efficacy endpoints … Read more
Is AI a threat to the medical writers of the World? With the hype around AI bots doing things humans once did, the question is an obvious one, echoing across every knowledge industry and sparking anxiety. Sophisticated algorithms can already generate succinct text and perform lightning-fast data processing, but can they replace the fundamental skill … Read more
For the last decade, the FDA emphasized that what matters most in modern drug development is the patient’s voice. The latest guidance on Patient-Focused Drug Development (PFDD) charts a detailed roadmap for integrating patient experience data into the heart of clinical trials. For drug and biologic sponsors, this isn’t just a regulatory update—it’s a strategic … Read more
For patients facing terminal or debilitating illnesses, time is not on their side. The FDA’s Expanded Access (Compassionate Use) program and the more recent Right to Try (RTT) pathway both offer hope when no approved therapies remain. As the FDA’s 2025 guidance reaffirms, decades of experience with compassionate use and the emergence of RTT have … Read more
