BLDE (DU) Site Management Office (SMO) is a reliable clinical trial-related site service provider to Contract Research Organisations (CRO), Pharmaceutical, Biotechnology and Medical device companies and others to enable them to deliver their research in a time-efficient and quality manner.
“To provide quality and value based clinical trials related site services to the clients across the globe.”
To ensure total quality management of projects and its deliverance within the stipulated timelines.
Adherence to the dynamic regulatory standards driven through the component of integrity, proactivity and transparency and trial subject centric work approach.
To enhance collaborative and synergistic endeavours to create best professionals and skilled manpower to meet the global clinical research industry requirements.
BLDE (DU) SMO has an adequate hospital infrastructure and a team of dedicated, experienced and expert staff in broader areas of therapeutics that will cater to and meet the client’s clinical trials research requirements in all domains of clinical research.
The SMO will aid in the delivery of operational and administrative support services to the clinical investigator at the research site. This includes everything from handling regulatory and compliance activities to managing patient recruitment and data collection. It can also provide support with study start-up, monitoring, and closeout and offer archival services as per client requirements. SMO offers the capability to ease operational complexity and regulatory compliance and allow research teams to complete on time.