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Press Releases

SANTA BARBARA, CA (PRWEB) October 7, 2014 – USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Grant Hodgkins, Vice President of Commercial Services and Solutions, will give a presentation about UDI Compliance at the Dental Trade Alliance Workshop. The workshop is 12:00 p.m. – 4:00 p.m. on Wednesday, October 8, 2014 in San Antonio, TX. The workshop will help dental manufacturers and distributors prepare to implement Unique Device Identification (UDI) and Automatic Identification and Data Capture (AIDC) for their dental products sold in the United States. Hodgkins will help dental manufacturers understand…
SANTA BARBARA, CA (PRWEB) September 25, 2014 – USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is proud to team with Oracle to give a presentation about Cloud solutions that meet regulatory compliance requirements for life science companies. The event is Tuesday, September 30, 2014 at 4:00 p.m. at Oracle OpenWorld. Attendees will have an opportunity to hear from Cloud security experts and gain knowledge about Oracle Cloud security and regulatory compliance. There will also be a chance to ask the presenters questions. “Validating the Cloud is extremely relevant and crucial for our clients,” said…
SANTA BARBARA, CA (PRWEB) July 16, 2014 - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Grant Hodgkins, Vice President of the company’s Commercial Solutions and Services, is a member of the GS1 Healthcare Leadership Team. Hodgkins was elected to the influential healthcare industry leadership team in early July. The team develops and maintains the GS1 Healthcare strategy for successful development and implementation of global standards. The group of industry leaders also helps develop the strategy to carry the GS1 standards message to government agencies that regulate the healthcare industry. “I am…
Partnership Helps Life Sciences Firms Increase Speed to Market While Ensuring 21 CFR Part 11 Compliance   SAN FRANCISCO—June 23, 2014 – DocuSign, Inc. (DocuSign®) and USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, today announced a new partnership to help organizations automate regulated business processes for dramatic ROI, increased security and compliance, and faster speed to market. DocuSign offers the industry’s only 21 CFR Part 11 compliant Digital Transaction Management (DTM) platform for easily, safely and securely managing transactions in the cloud, including clinical trials, electronic batch records, regulatory filings, training, change control,…
SANTA BARBARA, CA (PRWEB) June 11, 2014 - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is proud to announce Alfresco, Generis and USDM Life Sciences have partnered to offer a next generation Enterprise Content Management solution. The solution is able to meet existing and future life sciences organization needs while significantly lowering the overall cost of content management systems. Alfresco:The Alfresco content management platform eliminates information silos and provides quick and easy access to the right content from any system or device. With flexible on-premise cloud and hybrid deployment options, Alfresco places the power of…
SANTA BARBARA, CA (PRWEB) June 03, 2014 - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Jay Crowley, Vice President of UDI Solutions and Services and Grant Hodgkins, Vice President of Commercial Solutions and Services will share their insights regarding current challenges and opportunities in Unique Device Identification (UDI) and Pharmaceutical Track and Trace implementation at the GS1 Connect conference. Crowley will join the panel at the ‘GS1 Healthcare US Initiative Open Industry Meeting’ (session 148) where he will discuss the latest issues with UDI implementation. The presentation is June 10…
Jay Crowley Is the Architect of FDA's UDI Final Rule SANTA BARBARA, CA--(Marketwired - May 19, 2014) - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Jay Crowley, Vice President of UDI Solutions and Services, will give a presentation about UDI compliance at the UDI Implementation Workshop in Baltimore, MD. Crowley is scheduled to speak at 12:45 p.m. on Thursday, May 22. The UDI Implementation Workshop will help the medical device community become compliant with the FDA UDI Final Rule and offer guidance for the Global UDI Database (GUDID). Crowley…
Jay Crowley Is the Architect of FDA's UDI Final Rule   SANTA BARBARA, CA--(Marketwired - May 13, 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, is the keynote speaker at the European Diagnostic Manufacturers Association (EDMA) and Eucomed workshop called Implementation of a UDI System: A Focus on US FDA Rules. The event is from 9:30am - 4:30pm on Thursday, May 15th in Brussels, Belgium. Implementation of a UDI System: A Focus on US FDA Rules is a…
SANTA BARBARA, CA--(Marketwired - May 2, 2014) - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Diane Gleinser, Vice President of Operations will discuss validation of BioClinica OnPoint CTMS in an agile development environment at the BioClinica Global User Conference. Gleinser is scheduled to speak at 10:40am on Wednesday, May 7th. The presentation will include: Validation of BioClinica OnPoint CTMS under agile methodology Pros and cons of using agile methodology CTMS Validation cost savings of 40% - 60% "Validation of CTMS can be challenging under any circumstance. The agile methodology…
  SANTA BARBARA, CA--(Marketwired - Apr 15, 2014) - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, hires Grant Hodgkins as Vice President of the Commercial Practice. In his new role, Hodgkins will assist USDM Life Sciences clients with Pharmaceutical Track and Trace, Enterprise Resource Planning (ERP), Product Information Management (PIM), Product Lifecycle Management (PLM), Manufacturing Execution Systems (MES) and other commercial enterprise solutions. Hodgkins will also partner with Jay Crowley, Vice President of USDM's Unique Device Identification Practice to help clients achieve UDI compliance. Hodgkins has 29 years of experience as a leader in Global…

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