Reformulating an oral solid dosage (OSD) product can be challenging. Here are considerations for making sure you choose a CDMO partner with the right combination of experience, equipment, and technology for your drug product reformulation project.
Navigating regulatory requirements to achieve final approval and product launch can be a complex, time-consuming, and costly endeavor. How do you know your CDMO has the proper experience and capabilities to guide you through the submission process and support your post-approval needs? Here are some questions to ask.
Download our development and manufacturing solutions fact sheet to get the details on our facilities, capabilities from concept through commercialization, Category 3A/3B potency capabilities, regulatory approvals and registrations, and specializations.
Please fill out the information below to download the site fact sheet.