Developers and manufacturers of stem cell therapies need to understand how to conduct clinical trials in order to process FDA investigational new drug (IND) applications.
A MSO helps separate the medical side of a med spa from the business side of the med spa. A properly drafted MSA helps clarify the roles of the MSO and federal and state compliance issues.
The FDA’s Center for Biologics Evaluation and Research (CBER) regulates stem cell products. Stem cells normally require an investigational new drug application.
In today’s video, we’ll talk about a healthcare startup that wants to buy a medical or psychological or chiropractic practice and/or let’s just say partner with an MD, NP or RN, psychologist, or [...]
An update of California’s new laws such as AB 2178 that address many licensing, treatment, practice, and do’s and don’ts of the medical profession.