MSc Clinical research Course
Master
In Thane
Description
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Type
Master
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Location
Thane
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Duration
2 Years
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Start date
Different dates available
Clinical research is a branch of healthcare science that determines the safety and effectiveness (efficacy) of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving symptoms of a disease. Clinical research is different from clinical practice. In clinical practice established treatments are used, while in clinical research evidence is collected to establish a treatment.
The term clinical research refers to the entire bibliography of a drug/device/biologic, in fact any test article from its inception in the lab to its introduction to the consumer market and beyond. Once the promising candidate or the molecule is identified in the lab, it is subjected to pre-clinical studies or animal studies where different aspects of the test article (including its safety toxicity if applicable and efficacy, if possible at this early stage) are studied.
Facilities
Location
Start date
Start date
About this course
B.Sc Graduate Students
Graduates Science stream are now eligible to enroll for the above course. Working Professionals, Para Medics, MBBS, BAMS, BHMS, Pharmacists, etc.
B.Sc Graduate Students
RGULAR STUDY
CAMPUS STUDY
DOCUMENTS SCANED
APPLICATION FORM FILL
REGISTRATION CHARGES
Reviews
Subjects
- Clinical Study
- Clinical Physiology
- Clinical Nutrition
- Research
- World Studies
- Clinical Research
- Clinical Studies
- Clinical coding
- Clinical Pharmacy
- Clinical Psychology
Teachers and trainers (1)
SNEHA SHARMA
COUNSELOR
Course programme
- 1. Clinical Research
- 2. Clinical Trial management
- 3. Clinical Data Management
- 4. Data warehousing
- 5. SAS
- 6. Oracle Courses
- 7. Corporate Training in Clinical Research
Clinical trials involving new drugs are commonly classified into four phases. Each phase of the drug approval process is treated as a separate clinical trial. The drug-development process will normally proceed through all four phases over many years. If the drug successfully passes through Phases I, II, and III, it will usually be approved by the national regulatory authority for use in the general population. Phase IV are 'post-approval' studies.
MSc Clinical research Course