BioBridges has been engaged by an established, California-based, biotechnology company to provide regulatory medical writing expertise to act in a project management capacity, to support the development and workflow of protocols and additional documents, specifically for multiple clinical pharmacology studies, including internal review, comment consolidation, and resolution.
BioBridges provides clinical development services to emerging and established pharmaceutical, biotechnology and medical device companies. Since our inception in 2005, we have designed and built our proprietary and scalable Career Portfolio® Management model, which engages our professionals to meet the specialized needs of our clients’ clinical programs. This model has stood the test of time in our work with over 500 companies since our founding in Cambridge, MA. Today, we serve a national base of clients around the U.S. with our highly skilled professionals as we collaborate with our clients to advance science and produce therapies for patients who need them.
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