2024 - Unifying GxP Compliance: Digital Strategies for Biopharma Quality Systems
Date2024-06-12
Deadline2024-06-12
VenueONLINE-VIRTUAL, USA - United States
KeywordsLife Sciences; Pharmaceutical Regulation; Pharmaceutical
Topics/Call fo Papers
Discover an informative webinar focusing on why quality transformation is a top priority for life sciences companies.
Quality leaders at biopharma companies and their partners are seeking to turn their vision into reality by redesigning their legacy processes and modernizing their quality systems. Imagine unifying quality assurance (QA), quality control (QC) and manufacturing across applications, processes and partners.
Using a system that combines content management, training, quality management system (QMS) and laboratory information management system (LIMS) to accelerate quality processes across good x practices (GxPs) increases operational efficiency with standardization and automation, allows predictions and addresses quality issues before they occur; it also quickly adapts to new regulations and enhances visibility across the supply chain.
In this webinar, the speaker will share digitization opportunities and proven best practices that will help maximize quality management efficiency across quality and manufacturing.
Register for this webinar today to learn how to meet GxP compliance and redesign legacy processes and improve quality systems to increase operational efficiency in life science companies.
Keywords: Quality Control, Drug Development, CRO, Regulatory, Regulatory Affairs, Regulatory Compliance, Quality Assurance, Quality Management, GxP Compliance, GxP, Quality Management System, QMS, CDMO/CMO, Supply Chain/Logistics, Quality, Other Software
Quality leaders at biopharma companies and their partners are seeking to turn their vision into reality by redesigning their legacy processes and modernizing their quality systems. Imagine unifying quality assurance (QA), quality control (QC) and manufacturing across applications, processes and partners.
Using a system that combines content management, training, quality management system (QMS) and laboratory information management system (LIMS) to accelerate quality processes across good x practices (GxPs) increases operational efficiency with standardization and automation, allows predictions and addresses quality issues before they occur; it also quickly adapts to new regulations and enhances visibility across the supply chain.
In this webinar, the speaker will share digitization opportunities and proven best practices that will help maximize quality management efficiency across quality and manufacturing.
Register for this webinar today to learn how to meet GxP compliance and redesign legacy processes and improve quality systems to increase operational efficiency in life science companies.
Keywords: Quality Control, Drug Development, CRO, Regulatory, Regulatory Affairs, Regulatory Compliance, Quality Assurance, Quality Management, GxP Compliance, GxP, Quality Management System, QMS, CDMO/CMO, Supply Chain/Logistics, Quality, Other Software
Other CFPs
Last modified: 2024-06-12 05:09:03