Development & Strategy Clinical Development Planning

Clinical Development Planning

CTI offers a dedicated team of regulatory, medical, and operations experts to assist our sponsors in Clinical Development Planning. Our flexible staff is accustomed to partnering with our sponsors to develop plans that are not only sound from a regulatory perspective, but also take into consideration the goals of your organization. Our long-term relationships with several key thought leaders in our focused therapeutic areas result in knowledge of current trends in research and drug/device development around the world. Drafting a thorough and realistic Clinical Development Plan is a critical early step in the development process, and can lead to a productive platform for regulatory feedback to set your program up for success.

Dave Facklam, MS
Senior Director, Regulatory & Scientific Affairs
With more than 30 years of industry experience including strategic regulatory oversight, Dave has been directly involved in the writing and reviewing of marketing applications, and has made contributions to the development programs of several products on the market today including orphan and fast track designated products.

Dave Facklam

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CTI is ready to help bring your next drug to market

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