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Events

Chris Chandler, PharmD, Vice President of Healthcare Services and Solutions at USDM Life Sciences will speak among other pharmacy professionals at this year's ASHP Midyear Clinical Meeting & Exhibition during the Pharmacy Leadership Forum. 
China FDA (CFDA) continues to explore various options for the development and implementation for Chinese regulations on UDI. At the 6th annual China International Medical Device Regulatory (CIMDR) Forum, Jay Crowley opened the 2 day UDI Forum on September 22nd, and will speak on Wednesday, September 23rd. 
David Blewitt, VP of Cloud Compliance at USDM Life Sciences, will be a presenter of AppExchange for Life Sciences: Where the Cloud Meets Compliance at Dreamforce.
Thursday, September 17, 2015 from 4:00 PM to 8:00 PM (PDT)San Francisco, CA
Jennifer Mayes, Vice President of Business Development at USDM Life Sciences will be discussing USDM's wide array of client services and solutions pertaining to the regulated life science industry at the 2015 American Association for Clinical Chemistry (AACC) Annual Meeting & Clinical Lab Expo. 
A Knowledge-Based Program Thursday, May 28th - 6:00 p.m. to 7:00 p.m.Chris Chandler, PharmD Vice President of Healthcare at USDM Life Sciences Learning Objectives: Identify systems and processes that comply with the FDA Drug Supply Chain -Security Act (DSCSA) authorization and verification requirements after January 1, 2015. Cite the transaction documentation required for accepting product after July 1, 2015. Describe future implementation requirements for product serialization and traceability in the next decade. Recognize how recent FDA guidance documents affect implementation. Target Audience: Pharmacists, Physicians, Scientists, Post-docs, Pharmacy/Medical Students, Residents/Fellows, and Graduate Students. There is no fee to attend this program. A light dinner will be provided. If you wish to register please email Chris Shoemaker at cjshoema@uic.edu. TWO UNIVERSITY OF ILLINOIS COLLEGE OF PHARMACY LOCATIONS: LIVE PROGRAMChicago campus - 833 S. Wood St., Rm. 134-2, ChicagoLIVE BROADCAST Rockford campus - 1601 Parkview Ave., Rm. E226, Rockford The Drug Quality and…
Jay Crowley, Vice President of UDI Services and Solutions at USDM Life Sciences will speak at the session “Opportunity Beyond Compliance: Elevating Field Service in a Regulated Industry.” Jay will discuss moving beyond compliance to drive service excellence through ServiceMax and USDM’s UDI Connect app. Jay developed the framework and authored key requirements for FDA’s Unique Device Identification system. When: Thursday, May 14 at 1:45 p.mWhere: ServiceMax Maximize at Westin St. Francis in San Francisco
The extension for some implantable devices does not apply to all Unique Device Identification (UDI) requirements.  The extension only applies to the label requirement.  Requirements to collect, store, normalize, validate and submit data to the Global UDI database (GUDID) must be met by September 24, 2015. USDM Life Sciences will help you assess, plan and execute the changes and enhancements necessary to meet UDI regulations. Our team of UDI experts will assess your products, the markets where they are sold and determine an implementation strategy for the changes that need to be made. USDM’s assessment methodology is extensive and includes the labels and packaging, the management of identification changes to each product, the changes to PLM, ERP, EPCIS and packaging systems, changes to printing, vision inspection and warehouse/inventory management systems and interfaces to the GUDID.
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  • 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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