Professional Diploma in Clinical Trial Management :- Clinical research consists of testing and establishing the safety and efficacy of novel unapproved products, including biologics, medical devices and pharmaceuticals in human volunteers. Clinical trials in human volunteers are a pre-requisite for marketing approvals, by applicable regulatory authorities such as the U.S. Food and Drug Administration (FDA).
In addition to controlling and legislating clinical trial conduct, regulatory authorities delineate the principles by which clinical trials are to be taken-up. These principles are well known as Good Clinical Practices (GCPs).
Thorough knowledge of GCP guidelines and principles for the protection of human rights, prevention and discovery of fraud and the use of strong scientific principles is an essential requirement for a clinical research professional.
Whether you are taking into consideration a career in clinical research or by now working in the field, a certificate course designed to offer the training needed to presume the roles and responsibilities required to run clinical trials is a must.
This course helps you to master critical aspects of clinical trial conduct and management, along with clinical trial phases and design, scheduling, execution, data analysis, regulatory documentation and ethical considerations.
James Lind’s Professional Diploma in Clinical Trial Management program is so designed to cover the global requirements of proper clinical trial conduct. If you with to enroll Diploma in Clinical Trial Management please click apply now: 