Approaching IND: What To Consider In Early Development
Source: Cambrex

When preparing for IND submission, drug developers must carefully consider multiple components of their program: analytical challenges, manufacturing and engineering controls, delivery systems, and more. They must also take into account the facilities in which the development and manufacturing of their programs take place. Partnering with an experienced CDMO can help relieve some of the pressure from emerging biotechs as they manage these moving pieces.
In this webinar, Cambrex experts discuss tips for optimizing your early development program and the benefits of housing all related activities under one roof.
Key Takeaways:
- How to understand and prevent pitfalls that could impact your early-stage program
- Key components necessary for proper CMC data within an IND submission
- How to find the right CDMO to prepare your molecule for IND and beyond
access the Webinar!
Log In
Get unlimited access to:
Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue.
X
Enter your credentials below to log in. Not yet a member of Outsourced Pharma? Subscribe today.
Subscribe to Outsourced Pharma
X
Subscribe to Outsourced Pharma
Cambrex
This website uses cookies to ensure you get the best experience on our website. Learn more