Our services

We provide bespoke high quality clinical services specifically tailored to your needs.

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Clinical trials I to IV

Conducting clinical studies needs experience, highly committed people and established quality standards to meet the requirements of health authorities and to safeguard patient safety. The SSS team has been providing high-calibre clinical research services for more than two decades.

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Post-marketing studies

The requirements for post-marketing studies have become more demanding. Tight project control is needed now more than ever to provide effective management and support for large numbers of sites. SSS has long-term experience in conducting national and multinational non-interventional studies (NIS) and a proven track record of swift site and patient recruitment in sufficient numbers.

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Keeping to budgets and timelines is crucial in clinical trials. SSS has a valuable clinical network established in the course of clinical research experience spanning more than a quarter of a century. SSS assists clients right from the planning stages in areas including medical study design, statistical consultancy and sourcing services and vendors such as central labs and clinical trial suppliers.

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Medical devices

The Medical Device Regulation (MDR) and the In Vitro Diagnostic Device regulation (IVDR) will create a new pan-European standard, but clinical evaluation will be mandatory in many cases for manufacturers and diagnostic companies. As a seasoned provider with both the technical and clinical expertise required, SSS has what it takes to support companies every step of the way in planning and conducting clinical trials.

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The regulatory requirements for conducting clinical trials are subject to continuous change. Based on a deep understanding of legal standards and regulatory affairs, SSS hosts courses in Good Clinical Practice (ICH-GCP) for all clinical research team and sponsor project management roles.

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Drug safety regulations are continuously changing in response to growing demand for patient safety. SSS has a team of accredited and trained drug safety specialists who work in accordance with the current guidelines for central reporting via the EudraVigilance database.

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Data management and bio statistics

The outcome of clinical trials is all about data. Proper acquisition and processing and timely analysis allows us to generate insights early on in the process and to correct course as needed. Whether it’s a demanding phase I study in oncology or a huge phase III program, our flexible team of data experts and statisticians are ready to help you navigate the complexity of your trial.

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Medical writing

Medical writing requires special skills to produce well-structured documents that present medical information clearly and concisely. We have highly skilled scientific staff to create your study protocols, study reports, investigator brochures, publications and much more.

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