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."

Frequenty Asked Questions

Q: Are there really more than 8000 tasks and how can you possibly keep it all straight?
A: There are over 8300 tasks, and it is easy to keep them straight. The template is thoroughly organized into collapsible modules. It is surprisingly easy to navigate.

Q: How "authoritative" is this template?
A: Very. Some of the best minds in drug development have contributed to it. While no template can directly predict the nuances of a particular drug development program, you can be sure you'll have the vast majority of questions answered in terms of project management. Read the article in Applied Clinical Trials that highlights the value of using a template like this.

Download Template

You can download this template directly from this site and have instant access to knowledge that takes years to develop through day to day industry experience. Buy it now.

 

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