Attention Regulated Project Managers!

Avoid Surprises and Costly Delays in your Regulated Projects using Good Habits.

Click below to Register for the Manage Your FDA/EMEA Regulated Project Course

Here’s what is offered in the Manage Your FDA/EMEA Regulated Project course.

Ninety Minute Webinar

The key differences about Pharma and Med Device Projects will be covered, including the documents usually expected for Filing, Analytical, and Production. Insights will be given for planning a realistic timeline based on resources available, number of documents, and number of approvals needed for the documents.

 If you’ve never planned a project like this, you will have insight about setting up your first version of the timeline, so that you can refine it with your team.

 Also, you will use some tips on understanding how to manage shared resources, and perhaps shared equipment, as well as how to train/manage your sponsor.

 

Q&A

After the 90 minute course, one of hour of Q&A will be included.

 Use this opportunity to make sure you can “pull the thread” from understanding what you saw, and the examples, to apply in your situation.

Choose Your Date and Register!