Drug and medical device development is time-consuming and costly enough without extending the process or delaying progress through avoidable problems. Beyond carrying out trials under adherence to regulatory body requirements, Inamed also plays an important role in achieving client goals by streamlining efficiency, meeting critical milestones on schedule, maintaining communication, and delivering decisive data as soon as it’s available. With over one and a half decades of clinical research experience in Phase I to Phase IV trials, our clients benefit from streamlined operations across the entire study process from design up to the final study report.
Due to its strong scientific background and long-term expertise in planning and conducting clinical trials, Inamed's team of experts offers a broad spectrum of activities in the field of scientific and regulatory consultancy and services for clinical drug development with a focus on conceptual and strategic aspects consultancy.Read more
Regulatory requirements are continually evolving and further more vary from one country to another. To get the right strategy and moreover the different activities required across European countries in order to undertake clinical trials in line with national guidelines, our regulatory and clinical operation teams have extensive experience.Read more
Identifying, screening, qualifying and motivating investigative sites is an ongoing challenge for every clinical study. The more accurate the initial feasibility assessment for site identification the more successful the study.Read more
A Seamless Process From Start to Finish Integration and collaboration are the foundations of our superior statistical services. Inamed established a prolific relationship with a statistical company since 2011.Read more