Revamped Manufacturing Process Yields Fast-Track Ryplazim Approval Three Years Later
Executive Summary
Plasminogen therapy for unmet need licensed after Prometic took the time to develop a manufacturing process it could validate.
Topics
- Subjects
- Manufacturing
- Quality
- Drug Review
- Complete Response Letters
- Drug Approval Standards
- Biologics
- Regions
- North America
- Industries
- BioPharmaceutical
Latest Headlines
You must sign in to use this functionality
Authentication.SignIn.HeadSignInHeader
PS144537
Ask The Analyst
Ask the Analyst is free for subscribers. Submit your question and one of our analysts will be in touch.
Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.
All fields are required.
PS144537
Email Article
All set! This article has been sent to my@email.address.
All fields are required. For multiple recipients, separate email addresses with a semicolon.
Please Note: Only individuals with an active subscription will be able to access the full article. All other readers will be directed to the abstract and would need to subscribe.