Key Drivers To Overcome Obstacles In mAbs Formulation And Fill-Finish
Source: Avantor
By Jerry Keybl, Senior VP of Biopharma Products And Strategy, Avantor
Designing an effective, stable and safe high-concentration mAb formulation presents critical challenges for biomanufacturers. Despite selecting the right, compendial excipients for a balanced formulation, you may encounter obstacles in fluid handling, regulatory compliance and the supply chain that must be addressed to meet market deadlines. Discover the key strategies to overcome, aided by comprehensive support from suppliers, to streamline the formulation and fill-finish process and deliver effective mAb therapies on time.
access the Article!
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 Bioprocess Online? Subscribe today.
Subscribe to Bioprocess Online
X
Subscribe to Bioprocess Online
Avantor
This website uses cookies to ensure you get the best experience on our website. Learn more