A lifecycle approach can be used to develop GMP-compliant cleaning procedures for continuous manufacturing of solid-dosage pharmaceuticals. It is now possible, as demonstrated by Janssen (1), for drug ...

Data analytics, modular equipment, digital tools, and risk-based validation improve speed, flexibility, and quality. Many areas of pharmaceutical and biopharmaceutical manufacturing—solid-dosage drugs ...

DUBLIN--(BUSINESS WIRE)--Attend this "6-Hour Virtual Seminar On Qualification (Iq, Oq, Pq) And Validation Of Laboratory Equipment And Systems For Regulated Industries" webinar from anywhere which has ...

Qualification/validation can be defined as “establishing documented evidence which provides a high degree of assurance that specific equipment procured will ...

This seminar will provide valuable assistance to all regulated companies that need to review and modify their Master Validation Planning and Plan(s). While this information is focused on Medical ...

Amidst reports of doubtful credibility of manufacturing standards followed by some of the pharma companies in the country, particularly with reference to Ranbaxy, Hospira and Wockhardt, topics like ...