The Formulation Balancing Act: Overcoming Composition And Manufacturing Challenges
Source: Avantor
By Dr. Nandu Deorkar, Senior Vice President, Research & Development – Biopharma Production
The shift toward high-concentration monoclonal antibodies (mAbs) for subcutaneous injections is revolutionizing patient care, but it comes with significant formulation and manufacturing hurdles. This article explores how the right mix of excipients, stabilizers and buffers can minimize injection-site pain, while single-use technologies secure the fluid path to minimize contamination risks. Learn more about managing critical formulation challenges to pave the way for more patient-friendly therapies.
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