Life Sciences
Delivering solutions that support groundbreaking medical research and optimize business operations
Expediting the discovery and safe development of medical treatments and scientific advances
Our Life Sciences team employs a broad range of doctoral- and master’s-level scientific and analytical professionals who execute a diverse portfolio of biopharmaceutical, medical science, program management, and peer/program review contracts. From supporting ground-breaking medical research to optimizing business operations, we design and deliver customized solutions that help our customers perform more efficiently and overcome their most difficult challenges in healthcare.
Cancer & AIDS Research
Our science and technical staff conduct basic, translational, and clinical research and development in cancer and AIDS. We develop and apply new technologies in combination with leading-edge scientific capabilities in such areas as ultra-high-performance computing, nanotechnology, cGMP drug manufacturing, next-generation gene sequencing, and biomedical imaging at near atomic resolution.
Biomedical Product Development
Leidos Life Sciences executes a diverse portfolio of medical science, biopharmaceutical, and grant/program review contracts and has the ability to support all phases of manufacture, evaluation, and regulatory affairs for biologics, drugs, and medical devices. Our virtual pharma approach involves production and testing of vaccines and biotherapeutics for use in human clinical trials and utilizes a proven operating model that leverages the technical expertise of multiple CMOs, CROs, biotech firms and academia.
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Clinical Research Services
Leidos provides a broad range of clinical services and solutions to researchers, product sponsors, U.S. Government agencies, and other biomedical enterprises, hospitals, and health systems. We conduct efficient, innovative clinical research from initial planning to closeout and remain vendor-neutral while fostering and managing collaborations with the right clinical research partner(s) for your study. We can also advance your existing clinical research capabilities by incorporating real-world data such as electronic health records.
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VIEW CLINICAL RESEARCH TRANSFORMATION FACT SHEET
Quality & Regulatory Compliance
We develop, implement, and manage compliance strategies for pharmaceutical, biologic, and medical device manufacturers to help assure that their production facilities apply industry best practices and are in compliance with stringent FDA and international regulatory requirements. Among the services we offer: document preparation and control; quality program development and systems auditing; regulatory affairs consulting, compliance support, and gap and risk analysis; and training.
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Regulatory Affairs Support
Our Leidos Life Sciences team provides critical regulatory guidance at every step of the product development process to help accelerate product development. We help clients navigate the complex regulatory pathway from R&D to clinical trials and licensure, including assistance with document preparation and eCTD services.
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Biomedical R&D Program Management
Leidos executes a diverse range of program management services for biomedical R&D organizations to help them plan, manage, and defend their research programs. We offer scientific, technical, and business analyses for federal biomedical R&D organizations as well as portfolio management expertise and comprehensive capabilities in all phases of grant and contract management to provide practical strategies and solutions that help our clients meet their goals.
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Additional Life Sciences Support
Our diverse team of scientific, technical, and communication experts provide a broad range of additional capabilities including:
- A new service offering, the Leidos-Enabled Antibody Production Platform (LEAP2), that enables a one-stop monoclonal antibody development solution from bench-to-clinic.
- Our Online Review Information Network (ORION) platform that provides multifunction database support and interactive, customizable solutions to streamline meeting processes.
- A full-service publications and video/multimedia team with extensive experience producing high quality products ranging from regulatory submissions to effective communication tools in support of medical research programs and other federal customers.
Customers
