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Press Releases

 SANTA BARBARA, CA--(Marketwired - Apr 8, 2014) - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, will present a complimentary webinar titled Compliance in the Cloud: Solutions for Meeting and Maintaining FDA Regulations. The presentation is Thursday, April 17 at 11am PT/2pm ET. The live webinar will address critical issues life science companies need to be concerned about when moving regulated data to the Cloud. The presentation will feature a case study using USDM Cloud Assurance and 123Compliance to implement a complaints solution on Salesforce.com. The webinar will also highlight a case study on implementing…
Jay Crowley Is the Architect of FDA's UDI Final Rule   SANTA BARBARA, CA--(Marketwired - Mar 26, 2014) - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Jay Crowley, Vice President of the Unique Device Identification Practice, will discuss FDA UDI regulations at the Global GS1 Healthcare Conference in Seoul, South Korea. Crowley is scheduled to speak at 10:30 on Tuesday, April 1st. The Global GS1 Healthcare Conference is an opportunity for healthcare leaders to discuss worldwide efforts to improve patient safety, supply chain security and efficiency. Crowley will discuss…
Crowley Developed Framework and Authored Key Requirements for FDA's UDI System   SANTA BARBARA, CA--(Marketwired - Mar 17, 2014) - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Jay Crowley will host a complimentary webinar titled "Six Months Until UDI Go Live - Issues in the Life Sciences Industry." The presentation is Thursday, March 20th at 11 a.m. PDT. Crowley is Vice President of the Unique Device Identification (UDI) Practice at USDM Life Sciences. The live webinar will address critical UDI issues medical device manufacturers face and what to do…
SANTA BARBARA, CA--(Marketwired - Mar 4, 2014) - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Jay Crowley, Vice President of the Unique Device Identification Practice at USDM Life Sciences, will discuss UDI regulations at the Medical Device Manufacturers Association FDA Forum. Crowley will also discuss USDM's UDI solutions and services. "I'm looking forward to discussing how medical device companies should achieve UDI compliance and help them utilize the benefits of UDI," said Crowley. "USDM is uniquely positioned to help medical device companies become UDI compliant because of our well-established…
Jay Crowley is the Architect of FDA’s UDI Final Rule SANTA BARBARA, CALIFORNIA—(February 19, 2014) – USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Jay Crowley will speak at the Medical Devices Summit. Crowley will be a panelist at the “Understanding and Implementing Unique Device Identification” session on Tuesday, February 25th at 1:10 pm. “I am looking forward to helping medical device companies implement UDI in a way that not only achieves compliance, but helps them realize the global benefits of UDI,” said Crowley. As Vice President of the UDI…
Jay Crowley is the Architect of FDA’s UDI Final Rule   SANTA BARBARA, CALIFORNIA—(Marketwired - February 17, 2014) – USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Jay Crowley, Vice President of USDM Life Sciences Unique Device Identification Practice, will discuss UDI regulations at the GS1 Global Forum in Brussels, Belgium on February 17th at 16:15 and February 19th at 13:30. “As UDI rolls out globally, I’m looking forward to working closely with my colleagues at GS1 Global and the GS1 Member Organizations to help develop and implement global UDI…
SANTA BARBARA, CALIFORNIA—(Marketwired - February 12, 2014) – USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is proud to announce Brian McCole is now Director of the Enterprise Quality Management Practice. McCole is a highly experienced professional with a 20 year IT implementation track record. His experience includes 15 years of developing and supporting Quality Management System programs and 10 years of managing Enterprise Resource Planning system programs. He also has experience with business process improvement, regulatory compliance and the governance supporting technologies in the life sciences industry. Most recently, McCole was a Director…
SANTA BARBARA, CALIFORNIA—(Marketwired - February 5, 2014) – USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is proud to announce Kathleen Warner, PhD is now Vice President of the Project and Program Management Practice. Warner will use her Life Sciences management background to help USDM Life Sciences expand their project and program management services. Warner has over 25 years of experience as a professional manager, executive, trusted advisor and thought leader in Information Technology (IT) and Life Sciences. Over the years, Kathleen has managed large, complex, global organizations in a matrix environment. Over the…
Jay Crowley is the Architect of FDA’s UDI Final Rule SANTA BARBARA, CALIFORNIA—(Marketwired - January 29, 2014) – USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Jay Crowley, Vice President of USDM Life Sciences Unique Device Identification practice, will discuss UDI regulations at Oracle Value Chain Summit Wednesday, February 5th at 4 p.m. “I’m looking forward to discussing how medical device companies should move forward with UDI compliance and help them utilize the benefits of UDI,” said Crowley. “USDM is uniquely positioned to help medical device companies become UDI compliant…
Jay Crowley Is Now Vice President of USDM Life Sciences UDI Practice   SANTA BARBARA, CA--(Marketwired - Jan 8, 2014) - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce the FDA's UDI regulation developer, Jay Crowley will host his first complimentary webinar for the life sciences company. Crowley is now Vice President of USDM Life Sciences Unique Device Identification (UDI) practice. The webinar will outline what the UDI final rule means for medical device companies, offer tips for successful UDI compliance, address industry concerns and answer any questions participants have…

Testimonials

  • Clintrak - Jeffrey D. Coffin
    I have had the great pleasure to work with Bob for 5 years in his position of VP of Quality at Fisher Packaging Services while I acted as Director of Quality services at a sister…
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