Pharmaceutical and medical device manufacturers strive towards a culture of zero – zero hazards, zero defects, and zero waste. And Life Sciences 4.0 technologies hold great promise to help achieve this goal. However, the industry is significantly behind other advanced manufacturing sectors in implementing these technologies. At the same time, Life Sciences organizations must meet GxP requirements, update antiquated systems and processes, and address the demands of an increasingly tech savvy workforce.

This webinar will discuss the role that content management plays in pharmaceutical manufacturing to help companies reach the goal of zero in Quality and Manufacturing.
  • Learn how leading organizations leverage content management for GxP documentation
  • Hear about ways to improve documentation delivery to the manufacturing floor, labs, and warehouse
  • Better understand how new insights from real time data can accurately identify root causes to facilitate continuous process improvement

Featured Speakers

Deepa Kumar

Senior Solution Consultant

Deepa is a Lean Six Sigma Black Belt with a background in chemical engineering and biotechnology. She has 20 years of experience in the pharmaceutical industry in companies such as Human Genome Sciences, and GSK. In her career, she focused on biopharmaceutical process development, technology transfer,  strategy deployment, continuous improvement, coaching and change management in the biopharmaceutical R&D and manufacturing space. She recently joined OpenText as a Solution Consultant for the Americas Life Sciences team.

Ferdi Steinman

Life Sciences Industry Strategist

Ferdi Steinman has spent nearly 25 years driving strategy and commercialization efforts in biotech, pharma, and enterprise software with Fortune 500 companies such as Merck & Co, Eli Lilly & Biogen. Today, his focuses on strategic planning and industry marketing for enterprise software solutions.


Register now for this webinar