The main market opportunities include training on modern technologies for computer system validation, compliance with evolving FDA regulations, and risk-based approaches to validation using CSA and ...

DUBLIN--(BUSINESS WIRE)--The "How to Interview During GMP (Good Manufacturing Practice) Audits Training Course (Mar 12, 2026)" training has been added to ResearchAndMarkets.com's offering. Ensuring ...

India’s pharmaceutical manufacturing sector operates under one of the most stringent regulatory frameworks in the world. At the core of this framework lies Schedule M, which defines the Good ...

GMPs require high cleanliness and maintenance standards to prevent contamination and ensure product quality in pharmaceutical manufacturing. Risk-based maintenance programs focus on critical assets, ...

Proactive maintenance using digital tools and AI enhances GMP compliance, operational efficiency, and regulatory credibility. Facility design should integrate risk mitigation strategies, focusing on ...

The PHD Chamber of Commerce and Industry (PHDCCI), in association with the Department of Pharmaceuticals and the Kerala Branch of The Indian Pharmaceutical Association (IPA), is set to host a pivotal ...

DUBLIN--(BUSINESS WIRE)--The "How to Interview During GMP (Good Manufacturing Practice) Audits Training Course (Nov 10, 2025)" training has been added to ResearchAndMarkets.com's offering. Ensuring ...

This article is brought to you by our exclusive subscriber partnership with our sister title USA Today, and has been written by our American colleagues. It does not necessarily reflect the view of The ...

Greater Manchester Police WILL replace its failing computer system in 2027 — eight YEARS after problems first emerged. Cops have battled the ‘frightening’ PoliceWorks element of the force’s iOPS ...

The U.S. cannabis industry stands at a crossroads. With the federal government weighing whether to reschedule cannabis from Schedule I to Schedule III, operators, investors, and policymakers face ...

(MENAFN- GlobeNewsWire - Nasdaq) Emerging opportunities in drug/device combinations are driven by complex regulatory and quality challenges. These include clarifying EU/US definitions, understanding ...

During a NHP site licence assessment or a site inspection, a Health Canada officer or inspector notes deviations from Part 3 (GMP) of the regulations as explained in this guide. These deviations ...