Remove Engineer Remove Genotoxicity Remove In-Vivo Remove Marketing
article thumbnail

FDA’s New Draft Guidance on 510(k) Implant Devices: What You Need to Know

FDA Law Blog

Having a clear understanding of FDA’s data expectations for 510(k) applications related to implants is crucial for successful marketing clearance. Implant devices are used in a range of settings such as dental and orthopedic procedures. The intended duration of implantation is another crucial factor in performance testing.

In-Vivo 45
article thumbnail

Accelerating NDA filing through faster carcinogenicity assessment

Drug Discovery World

Due to the high costs associated with new drug development, pharmaceutical companies are under pressure to get effective drugs to market as fast as possible while ensuring they are safe for the intended patient population and dosing timeline, which can be lifelong for some drugs. billion and take over 10 years.