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5 Questions about Medical Devices


Did you know that the European Commission has adopted regulations for medical devices (MD) and in vitro diagnostics (IVD), replacing the previous EU Directives? Read this Medical Device Q&A to find out what impact the new regulations might have on your…

New Swelife-ATMP Regulatory Guide


Swedlife-ATMP is a project that provides expertise and support for Advanced Therapy Medicinal Products (ATMPs) from preclinical to clinical research and manufacturing. The project brings together academia, pharma, healthcare, and regulatory authorities and has a mission to increase awareness, identify…

Calmark Sweden AB signs an agreement with Scandinavian CRO regarding consulting services for clinical studies


Calmark Sweden AB has today signed an agreement with Scandinavian CRO, a Clinical Research Organization with vast experience and deep knowledge in the field of clinical studies. The agreement covers consulting services regarding the planning and execution of clinical studies…

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