11.08.11
Becker & Associates Consulting Inc. has tapped a former FDA staffer as one of it's most recent hires.
Tim Ulatowski, former director of the Office of Compliance within the Center for Devices and Radiological Health (CDRH) of the U.S. Food and Drug Administration (FDA), will service as director, Medical Devices, on the Becker's Expert Advisory Committee.
Ulatowski brings "significant pre-and post-market regulatory compliance expertise to the firm, and is available immediately to provide strategic guidance to FDA-regulated companies and their counsel," according to a release issued by the consulting firm.
Ulatowski has more than 36 years of public health experience, including more than 25 years in multiple leadership positions at CDRH. In addition to most recently serving as director of the Office of Compliance at CDRH, where he managed and supervised four divisions consisting of 180 staffers responsible for ensuring compliance with medical device laws and regulations, Ulatowski also has served as a primary reviewer on numerous 510(k) premarket notifications, investigational device exemptions, and premarket approval applications.
He also managed premarket activities as director of the Division of Dental, Anesthesiology, General Hospital, and Infection Control Devices at CDRH's Office of Device Evaluation.
In his new role, Ulatowski will provide guidance to the firm's medical device practice in addition to developing tailored technical consulting solutions for clients.
Based in Washington, D.C., Becker & Associates Consulting Inc. was established in 2002 and specializes in guiding corporations through the clinical and regulatory process.
Tim Ulatowski, former director of the Office of Compliance within the Center for Devices and Radiological Health (CDRH) of the U.S. Food and Drug Administration (FDA), will service as director, Medical Devices, on the Becker's Expert Advisory Committee.
Ulatowski brings "significant pre-and post-market regulatory compliance expertise to the firm, and is available immediately to provide strategic guidance to FDA-regulated companies and their counsel," according to a release issued by the consulting firm.
Ulatowski has more than 36 years of public health experience, including more than 25 years in multiple leadership positions at CDRH. In addition to most recently serving as director of the Office of Compliance at CDRH, where he managed and supervised four divisions consisting of 180 staffers responsible for ensuring compliance with medical device laws and regulations, Ulatowski also has served as a primary reviewer on numerous 510(k) premarket notifications, investigational device exemptions, and premarket approval applications.
He also managed premarket activities as director of the Division of Dental, Anesthesiology, General Hospital, and Infection Control Devices at CDRH's Office of Device Evaluation.
In his new role, Ulatowski will provide guidance to the firm's medical device practice in addition to developing tailored technical consulting solutions for clients.
Based in Washington, D.C., Becker & Associates Consulting Inc. was established in 2002 and specializes in guiding corporations through the clinical and regulatory process.