How ZenQMS + USDM can support your ZenQMS GxP Compliance. ZenQMS delivers a cloud-based eQMS platform purpose-built for life sciences organizations and designed for 21 CFR Part 11 / Annex 11 and relevant GxP/ ISO requirements from the ground up. The tool is easy to configure, validate and use, and it automates and enforces quality workflows ...27 Jul 2015 ... Open App. FDA's Drug Supply Chain Security Act - What You Need to Know Before Jan. 1, 2015. 971 views · 8 years ago ...more. USDM Life Sciences.Life sciences companies are aiming to boost innovation, quality, and speed with digitalization, new and evolving technologies, and third-party providers. However, these solutions may also introduce cybersecurity vulnerabilities. Security breaches target intellectual property and clinical trial data at life sciences companies and their third ...Employee Involvement Plan. The USDM OCM team analyzes your work streams to determine what activities can be used to build awareness and buy-in, then we identify change leaders who will help tailor messages to your broader internal audiences. Our OCM team will meet with a designated transformation leader bi-weekly to share …Lisa Om is the Vice President of Marketing and Communications at USDM Life Sciences, where… · Experience: USDM Life Sciences · Education: University of Colorado · Location: Denver ... In partnership with USDM Life Sciences, SAP S/4HANA allows regulated medical devices and life sciences companies to continuously meet all their compliance needs covering the solution and regulation simultaneously with our Cloud Assurance Subscription program. Any upgrade in the cloud is comprehensively assessed and supported to ensure the ... USDM Life Sciences has thorough processes, SOPs, and checklists to ensure that you follow the guidelines. We can also help you build a data integrity program that fits with your company’s priorities, plus: Assess and detect areas of risk. Remediate risks. Build a governance structure. Define a compliance strategy. Provide training programs.Using an automated compliance framework, USDM Life Sciences enables compliant change control with features like continuous monitoring, impact assessments, and updated automated tests for new releases and system updates. Compliance doesn’t have to be a burden—explore outsourcing options in this white paper > > >USDM Life Sciences today announced that ProcessX is now certified as part of the ServiceNow Built on Now™ program. Siloed technology systems for regulated and non-regulated workloads are a burden on IT and Quality teams. ProcessX helps minimize fragmented systems and processes to enable pharma, biotech, and medical … How ZenQMS + USDM can support your ZenQMS GxP Compliance. ZenQMS delivers a cloud-based eQMS platform purpose-built for life sciences organizations and designed for 21 CFR Part 11 / Annex 11 and relevant GxP/ ISO requirements from the ground up. The tool is easy to configure, validate and use, and it automates and enforces quality workflows ... Data is the lifeblood of AI. USDM helps your life sciences organization establish a data governance framework that ensures the integrity and security of your data as you apply AI to your business use cases. People are the weak link in responsible AI, but USDM provides the training and expertise to strengthen your position.USDM has been the exclusive life sciences compliance partner for Oracle for nearly two decades. As existing on-premises and new Oracle customers move their regulated data to Oracle Cloud, USDM’s Cloud Assurance program delivers a solution to enable these customers to achieve and maintain continuous compliance cost-effectively …Birds are beautiful creatures that bring life and melody to our surroundings. However, when they become a nuisance, causing damage to property or posing health risks, it’s importan...See full list on usdm.com USDM Life Sciences can help you think beyond cloud validation to enable platforms for innovation and new business models. We can help you: Empower data-driven decisions with artificial intelligence (AI) Today, product innovation is possible with the convergence of modern cloud technologies, development platforms, and AI.A GxP DevOps framework increases the frequency and quality of deployments to meet customer and business needs while automating compliance and security. It also enables a GxP-compliant software delivery pipeline. Read our case study to learn how USDM helped a Top 10 global pharmaceutical company create a validated DevOps …After decades of getting to know robotic animals through books and film, innovators have finally brought them into reality. Robots are everywhere these days. They can clean our hom...Lisa Om is the Vice President of Marketing and Communications at USDM Life Sciences, where… · Experience: USDM Life Sciences · Education: University of Colorado · Location: Denver ...USDM Life Sciences website. USDM Life Sciences provides a variety of IT and compliance solutions to help life sciences companies streamline laboratory, clinical and …and more. As part of application lifecycle management (ALM) in ProcessX, validation lifecycle management (VLM) generates all your validation artifacts automatically and compliantly using the Computer Software Assurance (CSA) methodology or Computer System Validation (CSV) methodology. You’ll receive: Validation plan. Requirements …At USDM Life Sciences, our purpose is to bring clarity and action at the interplay of technology and regulations to help biotech, pharma, and medical device companies deliver trailblazing outcomes. We help our customers utilize cutting-edge technology to increase their speed to market while ensuring continuous compliance and patient safety. Google, …Learn how USDM’s Managed Compliance Program drove standardization and efficiency for a global contract biopharmaceutical manufacturer in heavy acquisition mode. Anticipating Regulatory Compliance for Artificial Intelligence in Life Sciences | Whitepaper. Download Now. Search. Search. US: (888) 231-0816. [email protected]. …Nov 9, 2022 · EU MDR and IVDR Compliance. Medical device manufacturers must comply with EU MDR by May 26, 2021, and IVDR by May 26, 2022. USDM Life Sciences offers many solutions to help plan, execute, and manage any or all enterprise-wide activities necessary to meet the European Union (EU) Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation ... He has led projects & delivered solutions for Life Sciences including complex integrations for Supply Chain & Clinical Systems. A former solution architect and ERP integrator at Oracle, he is now a certified PMP with an excellent track record of project delivery including validations. Alex leads the Oracle Practice at USDM since 2019.USDM Life Sciences Summit 2024. ON DEMAND EVENT: AI is rapidly transforming the life sciences industry - but what are the practical use cases to get started today? These innovations bring new legal challenges related to intellectual property, data protection, regulatory compliance, and ethical considerations that must be addressed as you ...USDM Life Sciences is a consulting company that focuses on the life sciences sector. The company offers services such as automation of routine GxP workflows, cybersecurity, data integrity, and compliance management, all aimed at improving the interplay of technology and regulations. It primarily serves the biotech, …As USDM Life Sciences EVP, Europe I am the primary commercial manager of the European organization and entity USDM Europe GmbH.Prior to USDM, Kevin launched his career as a technology consultant. His passion for innovation, knowledge of enterprise technology, and entrepreneurial spirit have led USDM to become a leading digital solutions provider for regulated life sciences companies. Kevin’s leadership and commitment to the life sciences industry, has created a ...April 11, 2022. Content Orchestration is the seamless creation and management of content among teams in your organization. This phase of your cloud journey addresses your business need for centralized workflows, content, and data services that access GxP applications. This is a bigger concept than having a quality management system (QMS) …In today’s digital age, finding the perfect life partner has become easier than ever before. With the advent of online matrimonial platforms, individuals can now create their own p... DocuSign and USDM’s established partnership draws on expertise from deployments at the Top 20 global biopharma and medical device companies, and high-growth life sciences organizations. With USDM Cloud Assurance, you can use DocuSign to manage GxP validation. DocuSign can be used for HIPAA compliant signatures and data storage, 21 CFR Part 11 ... There are three main divisions of science: physical science, life science, and earth science. However, there are many subdivisions that also overlap, such as physical chemistry, as...SANTA BARBARA, CALIFORNIA – (November 16, 2021) USDM Life Sciences, a premier consulting firm driving digital transformation and innovation in technology and compliance, announces its first tailor-made event, Forward-Thinking GxP Compliance & Process Optimization, happening on Thursday, January 27, 2022. USDM, …In a complex, competitive, and fast-paced market, startups in biotechnology and biopharma, and early-stage medical device companies face many challenges on their journey from R&D to commercialization. Hosted by USDM Life Sciences in collaboration with Box, this virtual event provides valuable guidance and best practices to drive your compliance ...20 Feb 2023 ... Kevin Brown is the CEO of USDM Life Sciences. Kevin has more than 20 years of life sciences experience. Prior to USDM Life Sciences, ...Before USDM, Vega started a couple of companies and spent time on the boards of various non-profits. Vega was born in Denmark but has lived most of her life in California. She currently lives with her husband and two boys in Santa Barbara and enjoys spending time sailing, biking and hiking. She holds a BA in Political Science with International ...USDM Life Sciences has thorough processes, SOPs, and checklists to ensure that you follow the guidelines. We can also help you build a data integrity program that fits with your company’s priorities, plus: Assess and detect areas of risk. Remediate risks. Build a governance structure. Define a compliance strategy. Provide training programs.With more than 20 years of experience serving life sciences companies and delivering thousands of GxP projects globally, USDM can fast-track your Salesforce implementation, validation, and enhancements. Easily extend Salesforce to regulated functions like clinical, laboratory, R&D, quality, manufacturing, and other GxP areas.In a complex, competitive, and fast-paced market, startups in biotechnology and biopharma, and early-stage medical device companies face many challenges on their journey from R&D to commercialization. Hosted by USDM Life Sciences in collaboration with Box, this virtual event provides valuable guidance and best practices to drive your compliance ...The truth is that validation is a team effort. Achieving compliance and fitness for intended use pragmatically and efficiently requires a diverse mix of teams that spans the organization. It is common to face challenges when executing your initial plan throughout the validation lifecycle. Two critical challenges within the validation lifecycle are:Written by Chris Merriam-Leith, Director of Emerging Regulatory and Quality at USDM Life Sciences, Quality Management Systems for Emerging Life Sciences Organizations explains the benefits of aligning QMS practices with the top-down subsystem inspection approach taken by regulators. The U.S. Food and Drug Administration (FDA) …USDM Life Sciences is the most trusted company in the pharma, biotech, and medical device industries for compliant technology solutions. Enabled by USDM Cloud Assurance, we continue to build on this trust with our … USDM Life Sciences is a leading global consulting firm focused on life sciences. We specialize in regulated business processes, with an emphasis on compliance and performance. USDM Life Sciences provides innovative services and solutions that enable life science companies to achieve and maintain compliance across the entire enterprise. Hosted by USDM Life Sciences, this virtual event will help you apply Computer Software Assurance (CSA) guidance for a successful GxP cloud transformation, and senior leaders from regulated life sciences organizations will share ideas to advance your cloud compliance strategy wherever you are in your transformation. Fill out the form to watch …The life sciences industry’s quest for improved patient safety and product quality is heavily dependent on the use of technology throughout its business processes. The industry and the FDA are working together to optimize the process through which systems and technologies are validated. ... Learn how USDM can help you adopt … The final US UDI deadline will have passed (24 September 2022). The initial EU MDR/IVDR UDI label and package requirement deadline has also passed (MDR-complaint implantable and class III devices were 26 May 2021). More MDR and IVDR deadlines are fast approaching (e.g., MDR complaint Class IIa/b devices is 26 May 2023). With USDM Cloud Assurance You Can: All the functionality, none of the validation burdens, in one simplified web app. Always-On, total transparency to your IT systems state of compliance. Trusted solution by hundreds of Life Science organizations. Faster implementation and integration to maximize the ROI of your technology.Mar 8, 2024 · USDM Life Sciences is a company that helps life sciences companies use technology to increase speed to market and ensure compliance. Learn about their services, expertise, events, and leadership team. With more than 20 years of experience serving life sciences companies and delivering thousands of GxP projects globally, USDM can fast-track your Salesforce implementation, validation, and enhancements. Easily extend Salesforce to regulated functions like clinical, laboratory, R&D, quality, manufacturing, and other GxP areas. Say Hello to RPA. Robotic Process Automation (RPA) is software that acts like a robot (bot) to emulate how humans interact with digital systems to execute routine or repetitive business tasks. As the concept of RPA evolves, artificial intelligence (AI) can help automate complex processes and tasks, allowing AI robots to go from “execution ...18 Mar 2024 ... USDM Life Sciences is a premier consulting company with 20+ years of experience assisting heavily regulated biotech, medical device, and ...Feb 14, 2024 · Life Science Industry technology experts and innovators will be at Next ‘24 sessions to dive deep into: Accelerating molecule to market with leveraging validated and qualified generative AI modeling. Implementing a life sciences cloud native clinical data repository and data lake for regulatory submissions and gene therapy analytics. USDM ... At USDM Life Sciences, our purpose is to bring clarity and action at the interplay of technology and regulations to help biotech, pharma, and medical device companies deliver trailblazing outcomes. We help our customers utilize cutting-edge technology to increase their speed to market while ensuring continuous compliance and patient safety. Google, …Outsource Your Complaint and Adverse Event Management. Blog article topic: Learn the best practices to help get your complaint and adverse event program in place. USDM is a thought leader in the regulatory IT industry. We help life science companies make compliance easy. Read our blog for the latest tips! Oracle Supply Chain Management (SCM) & GxP Compliance. USDM Life Sciences and Oracle have partnered for more than 15 years to provide world-class solutions that enable life sciences companies to meet FDA 21 CFR Part 11 regulatory requirements. USDM delivers a trustworthy service that expertly manages GxP compliance for Oracle SCM customers. USDM Life Sciences has been conducting audits and assessments for the biotech, medical device, and pharmaceutical industries for more than 20 years. Our team of highly qualified auditors employs the Quality Systems Inspection Technique from the U.S. Food and Drug Administration (FDA). This helps to ensure your systems and processes meet ...USDM can manage your computer system, equipment, or process validation. We ensure that your systems are compliant from implementation to ongoing vendor updates. Quality Management Processes. USDM helps regulated life sciences companies make the best choices when selecting and integrating technology for GxP processes and applications.Jul 16, 2020 · The following ICH Q10 elements are required for successful implementation: Management review – helps to ensure that process performance and product quality are managed throughout the lifecycle. Process performance and product quality – monitored to maintain a state of control. Corrective and preventive actions (CAPA) – applied after ... USDM’s Vendor Assurance Report, an annual assessment driven by USDM’s proprietary USDM Compliance Matrix (UCM), assesses your compliance activities related to global regulations. USDM’s Cloud Assurance Certified technology vendors meet the quality and compliance demands of the life sciences industry. Our Talent, Fueled by Passion, Led with Purpose. Our team of subject-matter experts includes former FDA auditors and regulatory officials whose insight and oversight are part of every project. With superior industry knowledge and real-world experience, our multidisciplinary thought leaders possess the skills to address any opportunities or ... USDM Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender ... 3 days ago. Over 200 applicants. See who USDM Life Sciences has hired for this role. No longer accepting applications. About USDM. USDM Life Sciences is a premier …Kidney dialysis is a life-saving treatment for individuals with kidney failure. It plays a crucial role in removing waste products and excess fluid from the body when the kidneys a...USDM Audit of Google Life sciences and health tech companies are ultimately responsible for ensuring that their technology meets patient safety, data privacy, security, and compliance requirements; however, regulatory bodies realize the importance of the connection between the system owner and the cloud service provider. Some go as far as …USDM Life Sciences (also known as US Data Management) is a technology consulting firm. It offers regulatory compliance, digital transformation, and cloud assurance solutions. The company caters to medical device, biotechnology, biologics, diagnostics, and pharmaceutical industries.Mohamed is an accomplished regulatory and IS compliance professional with over 25 years in the life sciences industry. He has experience in computerized and automated systems for R&D, Production, Quality Management, Supply Chain, and Business Intelligence operations within FDA-regulated industries.This includes the process design, …A GxP DevOps framework increases the frequency and quality of deployments to meet customer and business needs while automating compliance and security. It also enables a GxP-compliant software delivery pipeline. Read our case study to learn how USDM helped a Top 10 global pharmaceutical company create a validated DevOps … USDM Life Sciences. Glassdoor gives you an inside look at what it's like to work at USDM Life Sciences, including salaries, reviews, office photos, and more. This is the USDM Life Sciences company profile. All content is posted anonymously by employees working at USDM Life Sciences. See what employees say it's like to work at USDM Life Sciences. USDM Life Sciences, Santa Barbara. 407 likes · 36 were here. Bringing clarity and action to the interplay of technology and regulations to help biotech, pharma, aUSDM Life Sciences has built its brand on core qualifications and validation services for pharma, biotech and medical device companies. But we don't stop there. We provide end-to-end services so that GxP and non-GxP customers build and implement the compliant systems they need to successfully compete in the industry.Life sciences organizations of all sizes struggle to manage cloud spending, technology bloat, and compliance burdens. Validation is complicated and time consuming, but it doesn’t have to be. ProcessX takes the ServiceNow platform , makes it 21 CFR Part 11 compliant, and simplifies compliance by achieving and maintaining IT and Quality regulatory …Joseph Cassella is the Director of Regulatory Compliance at USDM Life Sciences. With over 25 years of experience in the pharmaceutical, biotech, and medical device industries, Joe’s background is both broad and deep in Information Technology, Laboratory and Analytical Applications, and Quality Systems.Before USDM, Vega started a couple of companies and spent time on the boards of various non-profits. Vega was born in Denmark but has lived most of her life in California. She currently lives with her husband and two boys in Santa Barbara and enjoys spending time sailing, biking and hiking. She holds a BA in Political Science with International ...At USDM, Jay provides business process, technology, and compliance solutions for the regulated life sciences industry, and consults with medical device manufacturers to help them achieve regulatory compliance and a competitive advantage with UDI implementation. Lionel Tussau, Director, Strategic Industries, atrify. USDM is a trusted advisor and partner for life sciences organizations, offering solutions in IT, regulatory compliance, and domains. Learn how USDM helps over 700 customers in biotechnology, pharmaceutical, medical device, and other industries. USDM helps regulated life sciences companies make the best choices when selecting and integrating technology for GxP processes and applications across your enterprise. We excel at reducing implementation and validation time while optimizing your IT footprint and streamlining your QMS. While we take a technology-agnostic approach to meet your … USDM Life Sciences. 535 Chapala St. Santa Barbara, CA, US 93101. Europe +49 80 01777710. USDM Europe GmbH. The Squaire 12 – Am Flughafen 60549 Frankfurt am Main ... USDM's Cloud Assurance managed services for DocuSign provide a comprehensive implementation solution to meet 21 CFR Part 11 requirements. USDM helps life sciences companies rapidly deploy DocuSign to alleviate current business continuity and compliance bottlenecks. Achieve and maintain continuous cloud compliance and manage new …As USDM Life Sciences EVP, Europe I am the primary commercial manager of the European organization and entity USDM Europe GmbH.USDM is pioneering the integration of advanced AI models in life sciences organizations to help them generate dynamic content with text, images, and more. Our generative AI …Vice President, Consulting. Roger has over 20 years of experience in both consulting and industry roles in the pharma, biotech, engineering, and semiconductor industries. Working with small and large life sciences firms, Roger has built and led professional services teams to deliver solutions for customer needs and challenges.By KENX, Validation University is a 3 day conference that shares knowledge & best practices for validation in life sciences. 2024 Trends in Life Sciences - Learn about five trends fueling the industry | Whitepaper. Download Now. Search. Search. US: (888) 231-0816. [email protected]. ... who is presenting on Automation and AI for USDM ...11 Aug 2015 ... How to Avoid Common Pitfalls with Computer System Validation Projects. 1.7K views · 8 years ago ...more. USDM Life Sciences. Data-driven companies leverage cloud-based solutions for GxP and non-GxP data to develop new business models in their bold pursuit of innovation. Hosted by USDM Life Sciences, this virtual event will help you apply Computer Software Assurance (CSA) guidance for a successful GxP cloud transformation, and senior leaders from regulated life ... 30 Jun 2015 ... Implementing SAP Manufacturing Execution in Life Sciences Recording 08162012. 3.5K views · 8 years ago ...more. USDM Life Sciences. 489.18 Mar 2024 ... USDM Life Sciences is a premier consulting company with 20+ years of experience assisting heavily regulated biotech, medical device, and ...Employee Involvement Plan. The USDM OCM team analyzes your work streams to determine what activities can be used to build awareness and buy-in, then we identify change leaders who will help tailor messages to your broader internal audiences. Our OCM team will meet with a designated transformation leader bi-weekly to share … Holger Brämer is the EVP of European Operations at USDM Life Sciences. In this capacity, Holger is responsible for planning and executing business operations in Europe, overseeing revenue, growth, and profitability. He is located in Germany and serves as the main point of contact for all European customers and partners of USDM. Science has long been a cornerstone of human progress and innovation. From medical breakthroughs to technological advancements, scientific research has helped us understand the wor...Continuous Improvement and Audits: GMP is a dynamic process that encourages continuous improvement. Regular internal and external audits are conducted to identify areas for improvement, detect any non-compliance issues, and implement corrective actions. Good Manufacturing Practices are essential for ensuring the quality, safety, and …Cellular therapy products are regulated under 21 CFR Part 1271, 21 CFR Part 600, and 21 CFR Part 610. Drug manufacturing requirements in 21 CFR Part 211 and 212 also apply. Because of this, cellular products have unique concerns. One challenge is the reproducibility of product lots. Because your starting material for manufacture is …
USDM is a trusted advisor and partner for life sciences organizations, offering solutions in IT, regulatory compliance, and domains. Learn how USDM helps over 700 customers in biotechnology, pharmaceutical, medical device, and other industries. . Anthony edwards gotcha
Overview. 92. Reviews. 10. Jobs. 162. Salaries. 7. Interviews. 28. Benefits. 71. Photos. 19. Diversity. + Add a Review. USDM Life Sciences reviews. 3.8. 73% would recommend to …Jim has helped develop many of the regulatory compliance and IT programs at USDM including; our Unique Device Identification (UDI) program, EU MDR / IVDR programs, QMS strategies, complaint and adverse event support, RIMS initiatives and our Drug Supply Chain Security Act (DSCSA) compliance services for the medical device and …At USDM, Jay provides business process, technology, and compliance solutions for the regulated life sciences industry, and consults with medical device manufacturers to help them achieve regulatory compliance and a competitive advantage with UDI implementation. Lionel Tussau, Director, Strategic Industries, atrify.Vice President, Consulting. Roger has over 20 years of experience in both consulting and industry roles in the pharma, biotech, engineering, and semiconductor industries. Working with small and large life sciences firms, Roger has built and led professional services teams to deliver solutions for customer needs and challenges.Early-stage life sciences companies face many challenges, but a strategic IT roadmap doesn’t have to be one of them. This powerful tool helps you set and communicate your priorities, and you can adapt it as your circumstances evolve. Functional areas need IT solutions to meet their objectives and a strategic plan for needs, costs, and ...As life sciences companies progress in their automation maturity—from rule-based automation to virtual agents, cognitive agents, and AI/machine learning—USDM offers solutions to optimize use cases and applies computer software assurance (CSA) to drive efficiency. Watch the Automated GxP Cloud Compliance session from the USDM … USDM Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender ... Life sciences organizations of all sizes struggle to manage cloud spending, technology bloat, and compliance burdens. Validation is complicated and time consuming, but it doesn’t have to be. ProcessX takes the ServiceNow platform , makes it 21 CFR Part 11 compliant, and simplifies compliance by achieving and maintaining IT and Quality regulatory …Prior to USDM, Kevin launched his career as a technology consultant. His passion for innovation, knowledge of enterprise technology, and entrepreneurial spirit have led USDM to become a leading digital solutions provider for regulated life sciences companies. Kevin’s leadership and commitment to the life sciences industry, has created a ...USDM is pioneering the integration of advanced AI models in life sciences organizations to help them generate dynamic content with text, images, and more. Our generative AI services are finding applications in content creation, design enhancements, and decision support systems. Data Management. Elevate your data experiences with technology and ... If you bring the enthusiasm, motivation to learn, and self-starter attitude, USDM will bring the opportunities and growth!” - Organizational Change Management, Project and Program Management, Strategy, Emerging Erin Northington, VP of Emerging Life Sciences & Clinical Solutions USDM allows you to grow in ways that I never expected. Water is essential for human life, and the taste of water can vary depending on various factors. One of the most desirable tastes of water is sweetness. Sweeter water is not only m...Diane has over three decades of experience in the life sciences industry and leads a highly skilled team of implementation and compliance engineers. Her in-depth knowledge of the regulatory landscape and unwavering passion has been instrumental in rooting USDM’s focus on regulatory compliance for life sciences customers. Over her tenure ...Our Talent, Fueled by Passion, Led with Purpose. Our team of subject-matter experts includes former FDA auditors and regulatory officials whose insight and oversight are part of every project. With superior industry knowledge and real-world experience, our multidisciplinary thought leaders possess the skills to address any opportunities or ...USDM Life Sciences's annual revenue is $73.0M. Zippia's data science team found the following key financial metrics about USDM Life Sciences after extensive research and analysis. USDM Life Sciences has 350 employees, and the revenue per employee ratio is $208,571. USDM Life Sciences peak revenue was $73.0M in 2023.the industry to innovate and transform, and USDM Life Sciences (USDM) is providing an integrated compliance ... At USDM Life Sciences, our purpose is to bring ....