Sermes CRO has become the first Contract Research Organization to embrace Farmaindustria’s Code of Conduct for Personal Data Treatment
The company aligns itself with Farmaindustria’s guidelines, which oversee the handling of personal data in the realms of clinical trials and other clinical and pharmacovigilance research
ICH E9 and CDISC: The Master Formula for Excellence in Clinical Research and Data Management
Clinical studies play a key role in the development of new medicinal products and therapies, as well as in evaluating the efficacy and safety of existing medical treatments. To ensure the quality and reliability of the data collected in these studies, it is essential to follow robust guidelines and standards. One of the most important guidelines in this field is ICH E9, published by the International Council on Harmonization (ICH).
The CDISC Standards: The Success Formula for Clinical Data
In the world of clinical research, data exchange and analysis play a key role in the development of safe and effective treatments. The Clinical Data Interchange Standards Consortium (CDISC) have proven to be the formula for success in achieving effective harmonization and standardization in clinical data exchange. In this article, we will explore how CDISC standards have revolutionized the way data is presented, analyzed and shared in medical research, improving the quality of clinical trials and accelerating progress towards new therapeutic advances.