Clinical Trials
The clinical operations team is actively involved in the processes that carry out clinical studies. They begin by selecting the best study sites, are in charge of obtaining all necessary approvals, are responsible for preparing the study sites for study initiation, are present at the study sites 24/7 while the research is being conducted, and assist in archiving the study documents once the research is completed.
We can meet your clinical operation needs in India and South Africa with the help of our resources and local partner.
Clinical trials are an important part of drug development. ECR provides end-to-end services for Phase II to IV clinical trials on small medicines, drugs, nutraceutical products and medicinal devices, with fully ICH GCP compliant operations.
The difficulties that arise during all clinical projects are resolved on a regular basis by a group of skilled, experienced specialists who use their knowledge of therapeutics, regulations, and operational issues.
- Collection and clinical trial data
- Examine the case report forms and source documents.
- Ensure adherence to regulations
- Manage data queries resolution on time
- For site monitoring, ECR CRAs are committed and trained, imparting mastery of regional languages, norms, and operational processes.
- Our CRA teams offer rapid, most effective assistance for study sites and document management.
Clinical Trial Supply Management
ECR has the ability to store and distribute investigational drugs and clinical supplies. These services can be obtained alone, while they are frequently offered as a component of a full clinical services contract. All of our sponsors have audited our facility. As a result, we have been able to adapt our services to satisfy increasing regulatory and sponsor needs. To handle your unique needs, we have partnered with various logistics vendors.