Pediatric Patient Considerations During Dose Development
Source: Catalent

Pediatric clinical trials are becoming more prevalent and are now typically mandatory within clinical development plans. However, pediatric populations present significant development challenges related to dose form design. The absence of an available pediatric dosage forms can lead to increased potential for dosing errors or nonadherence. Therefore, specific dosing guidelines and acceptable dosage forms for pediatric patients need to be developed to optimize therapeutic efficacy and limit and prevent serious adverse side effects.
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 Drug Delivery Leader? Subscribe today.
Subscribe to Drug Delivery Leader
X
Subscribe to Drug Delivery Leader
This website uses cookies to ensure you get the best experience on our website. Learn more