MDC Associates, a leader in regulatory consulting and clinical study support for the in vitro diagnostics (IVD) and medical device industries, is reinforcing its clinical data management practice with the appointment of Sarika Reed as Director of Data Services.
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MDC Associates, a leader in regulatory consulting and clinical study support for the in vitro diagnostics (IVD) and medical device industries, is reinforcing its clinical data management practice with the appointment of Sarika Reed as Director of Data Services. Reed brings over a decade of experience in clinical data management and is known for her expertise in database development, data quality assurance, and regulatory compliance. Her leadership supports MDC’s mission to help clients achieve regulatory success through improved robust clinical data strategies. Reed’s addition underscores MDC’s commitment to streamlining data management processes to deliver accurate and efficient results for clinical trials, enabling clients to navigate complex regulatory landscapes with confidence.
Accurate and efficient clinical data management is a key component of the comprehensive suit of support services that MDC provides to the IVD and MedTech industry. With decades of experience supporting clients and clinical studies in the United States and Europe, MDC Associates is well-positioned to address the complex data management needs of its clients. In response to growing industry demand, the Data Team at MDC offers a number of customized services including customized data strategies, electronic data capture (EDC) systems, and database design.
Reed joins MDC with experience at Medrio, DePuy Synthes, and NuVasive, where she led clinical trial database development and data-driven strategies to support regulatory submissions. Her technical acumen and leadership have consistently delivered outcomes that meet regulatory standards. Reed also holds a B.Sc. in Bioengineering from UC San Diego and a Biostatistics Certificate, providing her with a strong foundation in data analytics and clinical trial management. Her background in optimizing data management processes will strengthen MDC’s ability to support clients in achieving efficient and compliant clinical trials.
About MDC Associates:
MDC Associates is a trusted partner for in vitro diagnostic (IVD) and medical device companies, providing tailored regulatory, quality, and clinical study solutions to navigate the complex path from development to market approval. With decades of experience, MDC specializes in supporting diagnostic technologies across microbiology, infectious disease, clinical chemistry, and companion diagnostics, offering expertise in high-complexity assays, CLIA-waived tests, and over-the-counter (OTC) products.
Headquartered in the Greater Boston Area, MDC Associates operates as an extension of its clients’ teams, going beyond strategy to actively execute regulatory submissions, quality systems implementation, and clinical trial management. By emphasizing collaboration and precision, MDC helps clients demonstrate the safety and efficacy of their products, ensuring compliance with FDA and international standards.
Through a client-focused approach, MDC is dedicated to advancing healthcare by supporting the development of life-saving diagnostics and medical technologies that improve patient outcomes worldwide. For more information, visit www.mdcassoc.com.
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Release ID: 89147824
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