Anuh Pharma’s manufacturing facility found compliant during EDQM regulatory audit: Our Bureau, Bengaluru Wednesday, March 11, 2026, 16:30 Hrs [IST] Anuh Pharma has cleared the g ...
Dr. Reddy's Laboratories has received the Establishment Inspection Report (EIR) from the U.S. Food and Drug Administration ...
Dr Reddy’s Laboratories said the USFDA has classified the inspection of its Srikakulam formulations manufacturing facility as Voluntary Action Indicated (VAI) and issued the Establishment Inspection ...
Two men have been jailed after a police chase involving a lorry containing more than £40,000 worth of stolen tyres ended near Bradford.
Concept paper on the revision of Annex 6 - Manufacture of medicinal gasesThe Pharmaceutical Inspection Co‑operation Scheme (PIC/S) have opened a ...
BioAnalysis launches BASIS 2.0, its next-gen GMP-compliant AUC software for gene therapy. Higher throughput, one-click ...
Environmental monitoring is a cornerstone of pharmaceutical manufacturing, ensuring product quality, patient safety and regulatory compliance across both sterile and non-sterile operations. Yet many ...
PAI took place over four days for an API that the Malvern, PA site will manufacture for a global pharma company.
Smruthi Organics Limited has received an "Attestation of Inspection" from the European Directorate for the Quality of Medicines & HealthCare (EDQM), Council of Europe, following the inspection ...
Holland & Barrett’s Global Production Centre is rapidly redefining what contract manufacturing looks like in the health and ...
Cell therapy manufacturing is uniquely vulnerable to contamination, variability, and operational burden because the product - ...
Q4 revenue of $38.9 million, total revenue of $70.4 million for the fiscal year ended December 31, 2025 Ended year with $78.2 million in cash, cash equivalents and short-term investments, runway ...
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