CMC Writing and Submission Strategies: A Global Regulatory Approach
By Shrinivas (Cheenu) Murti
Published in: CFPA Course
Published on: October 10, 2019
This 12-hour accredited training, will provide in-depth instruction on Chemistry, Manufacturing and Controls (CMC) requirements and review processes for clinical trial, registration and post approval drug applications in the US, Europe, and Japan.
If you have not yet signed up for the StabilityHub newsletter, join hundreds of other stabilitarians to get the latest news, publications, job opportunities and more!
By submitting this form, you are consenting to receive emails from: StabilityHub, You can revoke your consent to receive emails at any time by using the SafeUnsubscribe® link, found at the bottom of every email. Emails are serviced by Constant Contact