As the pharmaceutical landscape becomes increasingly complex, the US Food and Drug Administration (USFDA) has definitively shifted from a purely reactive, punitive compliance model to a proactive, risk-based oversight framework. This strategic evolution, championed by the principles of ICH Q9…
As the pharmaceutical landscape evolves, so too does the rigor of the U.S. Food and Drug Administration’s (FDA) oversight. The Pre-Approval Inspection (PAI) e.g. USFDA PAI checklist remains the critical gatekeeper, serving two primary objectives: to verify the authenticity and…
The landscape of endocrine therapy for hormone receptor-positive (HR+) breast cancer continues to evolve rapidly, particularly for patients whose disease has become resistant to standard-of-care treatments. On September 25, 2025, the FDA approved INLURIYO (imlunestrant) tablets, a new oral selective…
In the rapidly evolving landscape of regulated industries, 21 CFR Part 11 compliance remains a cornerstone of digital transformation and regulatory adherence. This USFDA regulation establishes the criteria under which electronic records and electronic signatures are considered trustworthy, reliable, and…
A USFDA Warning Letter (WL) is more than a mere correspondence; it is a public declaration of significant non-compliance with the Federal Food, Drug, and Cosmetic Act, posing an immediate, existential threat to a pharmaceutical, medical device, or biologics operation.…
For global pharmaceutical and medical device manufacturers, particularly those operating in high-volume markets like the US and India, the receipt of an FDA Form 483, Inspectional Observations, is not merely a documentation step—it is a critical inflection point. In the…
For pharmaceutical manufacturers, especially those eyeing the lucrative United States market, USFDA pharma compliance and Inspection readiness is not merely a regulatory hurdle; it is the cornerstone of commercial viability and corporate reputation. The U.S. Food and Drug Administration (FDA)…
The U.S. Food and Drug Administration (FDA) granted Accelerated Approval to FORZINITY (elamipretide) on September 19, 2025, marking a pivotal moment as the first approved treatment for Barth Syndrome (BTHS) in eligible patients. This rare, X-linked, infantile-onset disease previously relied…
In a significant development for oncology practice, the U.S. Food and Drug Administration (FDA) on September 19, 2025, granted approval for Keytruda Qlex (pembrolizumab and berahyaluronidase alfa-pmph), a new subcutaneous formulation of the widely used PD-1 inhibitor, pembrolizumab. This approval…
On August 12, 2025, the U.S. Food and Drug Administration (FDA) approved Brinsupri (brensocatib), a novel, first-in-class dipeptidyl peptidase 1 (DPP1) inhibitor for the treatment of non-cystic fibrosis bronchiectasis (NCFB) in patients aged 12 and older. This approval marks a…