SDS Life Science - a Cytel company

www.sdslifescience.com

SDS Life Science is a Swedish company founded in 2012 and, since 2022, part of Cytel Inc. We supply the pharmaceutical industry with consultancy services in drug development, regulatory affairs, biostatistics, clinical project management, and real world evidence. Together with our sister company SDS MedteQ, which focuses on medical technology services, we have over 60 employees and a Ph.D. rate of over 50%. In 2021, we were ranked as Sweden’s 11th best employer in the category of small enterprises, according to Great Place to Work. We provide expert advice on formulation development, clinical and non-clinical program planning, and therapeutic product development. Our experienced project managers can provide all the necessary support and oversight of activities for the program, including writing the protocols and technical documentation. We have experts in writing high-quality clinical reports that meet the authorities’ standards. In addition, our trusted team of regulatory experts can act as communication mediators with regulatory authorities. In collaboration with our regulatory experts, our statisticians help clients conduct well-designed studies per the regulatory standards.

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SDS Life Science is a Swedish company founded in 2012 and, since 2022, part of Cytel Inc. We supply the pharmaceutical industry with consultancy services in drug development, regulatory affairs, biostatistics, clinical project management, and real world evidence. Together with our sister company SDS MedteQ, which focuses on medical technology services, we have over 60 employees and a Ph.D. rate of over 50%. In 2021, we were ranked as Sweden’s 11th best employer in the category of small enterprises, according to Great Place to Work. We provide expert advice on formulation development, clinical and non-clinical program planning, and therapeutic product development. Our experienced project managers can provide all the necessary support and oversight of activities for the program, including writing the protocols and technical documentation. We have experts in writing high-quality clinical reports that meet the authorities’ standards. In addition, our trusted team of regulatory experts can act as communication mediators with regulatory authorities. In collaboration with our regulatory experts, our statisticians help clients conduct well-designed studies per the regulatory standards.

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City (Headquarters)

Stockholm

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Founded

2012

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Potential Decision Makers

  • Chief Executive Officer

    Email ****** @****.com
    Phone (***) ****-****
  • Director Clinical Project Management

    Email ****** @****.com
    Phone (***) ****-****
  • Director Regulatory Affairs

    Email ****** @****.com
    Phone (***) ****-****
  • Regional Director

    Email ****** @****.com
    Phone (***) ****-****

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