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Monitor Clinical Trials
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Smile Monitor Clinical Trials - 01-03-2013, 05:38 AM

Hi Community,

1. Review the clinical trial protocol provided by the company sponsoring the research.

2. Determine the frequency and amount of monitoring required for the study. This is based upon several factors such as the study's complexity, disease state, number of subjects enrolled, site's performance and experience and the rate of enrollment into the study. The company sponsoring the study may also have guidelines that must be followed for monitoring.

3. Begin visiting the clinical trial site after the first subjects are enrolled in the study. Ensure protocol procedures are being followed and that the site staff understand all applicable procedures.

4. Complete the site monitoring report provided by the sponsor for each visit. Verify and complete all items listed in the report.

5. Submit the monitoring report to the clinical trial sponsor and the appropriate regulatory authorities. Ensure any issues that were observed during the monitoring inspection are addressed in conjunction with the sponsoring company. This will ensure the trial progresses according to the applicable guidelines.

Regards
Lucy James

Patient Enrollment In Clinical Trials
   
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Default 01-25-2013, 10:51 AM

Hi
Welcome to this forum site . This is best site .

I want to go for clinical trial .... how can i do ?


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Default 01-26-2013, 10:10 AM

Welcome in the forum will check the sources of you.
   
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Default 01-28-2013, 09:50 AM

This type of pharmaceutical quality control training can prepare you to oversee clinical trials for a large pharmaceutical company.
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