Webinar: Enterprise Solutions for Full Drug Lifecycle
Sponsored by: Infotehna
Focused on:
Date: 22rd June
Days old: 4977
Time: London 3PM / New York 10AM
Addressing Challenges in Today's Market
Life sciences companies face undaunting challenges in todays market. While recognizing the importance of drug life cycle management, too often manual processes still dominate their internal processes.
To achieve ultimate market success, companies must embrace automation to effectively drive the drug lifecycle process. These challenges increase as markets approach the mature and declining stages and generics competition looms.
This webinar will focus on challenges, opportunities, and enterprise automation designed exclusively to help companies effectively manage the drug lifecycle process. Today's life sciences organizations create, use and manage a broad array of of documents across the drug life cycle process. At the core of any drug lifecycle management process is a robust content management system designed to address the unique business and regulatory challenges faced by companies.
You will learn how leading companies today are leveraging advanced technology to accelerate the drug life cycle process and lower technological total cost of ownership.
Presented by
Valarie King-Bailey, MBA,
Sr. Industry Consultant, Life Sciences Infotehna
Valarie presently serves as the VP U.S. Sales and Marketing for INFOTEHNA, world leader in the development and deployment of Enterprise Compliance Management systems.
Ms. King-Bailey has over 25 years of extensive technical and marketing experience within the process industry. Prior to her her tenure with INFOTEHNA, Valarie’s marketing efforts helped her former employer QUMAS to win the prestigious honor of being shortlisted for the 2001 Software Industry Marketing Innovation Award and Software Industry Company of the Year Award sponsored by Enterprise Ireland. She also served as Director of Document Management & Quality Systems for Abbott Laboratories Hospital Products Division leading the design and development of regulatory document management systems.
Valarie received the prestigious Abbott Chairman’s Award for two consecutive years and the Abbott Hospital Products Division Value Leadership Award for her efforts. Prior to Abbott, Valarie served as Director of Industry Development for Documentum where she led the development of DocControl Manager, Documentum’s first off-the-shelf product. Valarie is an expert in the area of regulatory compliance, document management and electronic records management. She is a frequent guest speaker at RAPS, DIA, MER, Institute of Validation Technology, Institute of Quality Professionals, and many other regulatory industry forums around the world.
She holds a Master of Business Administration (MBA) in Information Systems from Keller Graduate School of Management in Chicago and a Bachelor of Science degree in Civil and Environmental Engineering from the University of Wisconsin - Madison. She received the Distinguished Alumni Award from the University of Wisconsin College of Engineering and a Lifetime Achievement Award From the College of Civil and Environmental Engineering. Valarie is based in Chicago, Illinois.
Download Slides
Please login to download the slidesKey Learning Objectives
- How to Accelerate new drugs to market
- eCTD Advantages and Challenges
- Ensuring compliance with ICH and global regulations
- Improving Submission ROI
Audience
- Senior Executives
- Departmental Heads
- Directors
- Heads of Regulatory Affairs
- Research and Development
- Quality Assurance
- Quality Control