Comprehensive Drug Development Project

Comments

"Knowing how to integrate CMC with Noncliniical and Clinical helps me to communicate better with those departments."

"It helps me keep the full scope in view, all the time."

"The regulatory backbone keeps us focused on what FDA and EMEA really need vs. all the questions we'd like to address in our development."

"It is so visual with the Gantt charts. I really like how the modules are organized.. how they unfold and collapse."

"All the specific, task-driven content and good explanations of what triggers which task...those are the biggest benefits."

"It's like having an industry guru on your desk, without having to pay outrageous consulting fees."

"It's a lot better than the plan we use internally. It comes from a different approach and has just the right amount of detail."

Features:

  • 13 modules covering the entire drug development process, from Discovery through Product Launch
  • Expert-based task links for cost-control and project time efficiency
  • Over 8300 tasks organized in easy-to-manage collapsible modules
  • Comprehensive regulatory backbone to meet FDA and EMEA requirements
  • Predecessor task triggers are labeled for easy identification rather than hard-to-follow task numbers
  • Built in Microsoft Project and works in versions 2002 and above

Benefits:

  • Keep development teams focused
  • Minimize surprises
  • Maintain control of budgets
  • Reduce costs
  • Speed up development cycles
  • Train team members

Price:

  • Single User License US$995, Six User License $3995, Enterprise Unlimited License $14995
  • Visa, Mastercard, Discover, Amex accepted (Option to pay by check)
  • Download file from emailed secure link following payment

License Selection

 
Single User US$995

Up to Six Users US$3995

Enterprise Unlimited US$14995

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