Expert Research Support 

We provide custom research to satisfy compliance obligations and support decision-makers in the pharmaceutical and medical device sectors. We cooperate with the Client to define research strategy and objectives to serve business needs. On behalf of our clients, we perform screening of relevant data sources, including scientific literature, and prepare summaries and compile reports for regulatory submission or internal purposes. 

• For Device manufacturers, we screen scientific literature and compile summaries to support clinical evaluations, post-market clinical follow-up, and biocompatibility assessments. 

• We support literature screening and summaries for PSURs (GVP Module VII), DSUR (ICH E2F), study protocols, and ad hoc background research for the Pharma industry. We provide CONSORT-compliant study summaries, Summary of Findings tables, and grade evidence using Cochrane tools. 

• We provide scientific information support for management boards and investors in the life science, medical technology, pharma, and biotech sectors.