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SLE nephritis is common , treatment should be started as soon as diagnosis . Treatment is divided in...
In any work or process documents that are needed before initiation, Between or generally the end of ...
A Data Management Plan (DMP) describes data that will be acquired or produced during research; how t...
CDM is defined as the process of collection, cleaning, and management of subject data in compliance ...
TSDP tells about the essential documents that are required for the #conduct of a clinical trial. For...
This presentation is a brief overview of ICH-GCP guidelines. Although ICH-GCP is a very vast topic, ...
Essential documents for conduct a clinical trials
Infectious Diseases Journal Club 4-11.pptx
Cross trial esophagus updated result
Life Cycle of Clinical Trials
Clinical research associate responsebility
clinical trial approaches with clinical trial management under ethics committee
for the better understanding of the student
CARCINOMA ENDOMETRIUM PORTEC TRIAL
IRB REVIEW
Trastuzumab in her2 positive breast cancer
Dr. Merrin Joseph,Department of pharmacy practice,Institutional Review board /Research and ethical c...
clinical trail documentation
This presentation enumerates the responsibilities of various clinical trial players whilst managing ...
IRB/IEC
GCP is a set of guidelines for how clinical trials should be carried out. It ensures that the data...
Recent advances in the pharmacotherapy of Non-Alcoholic Steatohepatitis (NASH) have made significant...
PORTEC TRIAL
Kiran Rajput MSc. Clinical Research 4th Semester
