Skip Ribbon Commands
Skip to main content
Sign In
Skip Navigation Linksvmc.com > Solutions & Services > Industries > Health and Life Sciences
Case Study: Agile Test-Driven Development

When a leading provider of wireless communication networks to the railroad industry was awarded a federally-funded contract and needed to ramp up quickly, they turned to VMC to implement a sustainable, scalable infrastructure for Agile development while simultaneously achieving critical software development milestones.

Case Study: Server Technical Support

When a global technology company needed a high- quality inbound telephone technical support team to provide the company’s Premier and Professional customers with timely, effective IT assistance throughout North America, Latin America and Europe, they outsourced to VMC.

1 - 2 Next
 

Health & Life Sciences

VMC assists health and life sciences companies in meeting the demanding requirements of regulatory agencies by providing support services for data management, bio statistics, technical writing, computer system validation and clinical research. Through the use of people, processes and technology, VMC is able to increase productivity and overall efficiencies in the execution of projects that require compliance under the rules and guidelines of the United States Food and Drug Administration (FDA). VMC is well versed in serving the unique issues of health and life sciences companies, combining our practical experience, intellectual capital of industry knowledge, understanding of the rules and regulations, and listening to the voice of our customers. Clients benefit from this competitive advantage through a best practices approach that matches the needs of our health and life sciences clients with regulatory demands.
 
VMC delivers U.S. FDA compliant testing, validation and technical writing for health and life sciences companies. Our experience and understanding of processes and requirements working under FDA regulations enable us to extend valuable resources to research and development programs at medical device companies, pharmaceutical companies and other biomedical companies, following Good Manufacturing Practice (GMP) matters. Our lab management and sample management provide outsourced lab environments under client direction of priorities, with safety plans, easy record access from a secure environment, training and testing to meet the needs of our clients.
 
From Standard Operating Procedures (SOP) to tool documents and specific job aides, our services are conducted within the standards of the FDA on behalf of your company. Our technical writing expertise includes clinical trials, molecular submissions, internal collaborative content and knowledge share (SharePoint sites) creating a “one stop shop” for accessing the most current tools and procedures. Our lab environments offer document storage in a secured repository, logistical data sharing, certificates of analysis (CofA), procedure tools, and versioning control of many types of documents in secured document repositories, serving as a source for historical information. Our validation services team assures results in accordance with quality and purpose. Our testing is executed according to requirements and design documents, with implementation of preapproved test scripts in a sandbox environment. We execute approved test scripts with commentary, knowing that if a step fails, the script fails, so that we can assist with revised test script writing and complete documentation for the test summary report. VMC will help you streamline acceptance testing within FDA regulation standards, improving your productivity and timelines.
 
Let VMC help you navigate the road to FDA compliance with testing, validation and technical writing services for health and life sciences.