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  • Clinical Research SOP and Report writing

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    4. Clinical Research SOP and Report writing
    1-SOP on writing a Confidentiality Agreement
    Summary
    2-SOP on writing an investigators brochure for clinical trials
    Summary
    3-SOP on the Maintenance of the study site master file
    Summary
    4-SOP on Procedure for drawing blood
    Summary
    5-SOP on Measuring Vital Signs in Clinical Trials
    Summary
    6-SOP on establishing the process for reading and implementing a clinical research protocol
    Summary
    7-SOP on Implementing the informed consent process for clinical trials
    Summary
    7-Assignment for writing an Informed Consent Form (ICF) for a study protocol
    8-SOP on Managing source documentation
    Summary
    9-SOP on Study Visits and Missed Visits
    Summary
    10- SOP on Managing Study Medications
    Summary
    11-SOP on Managing Subject Recruitment for Clinical trials
    Summary
    12-SOP on Toxicity Management, AE and SAE Reporting
    Summary
    13-SOP on Managing subject logs and codes
    Summary
    14-SOP on Assigning and Management of Patient and Study Identification Number.
    Summary
    15-SOP on Performing Patient Screening and Enrollment
    Summary
    16-SOP on Conducting Study Monitoring Visits
    Summary
    17-SOP on Writing a Clinical Study Protocol (2 weeks)
    Summary
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          • SOP writing

          • Clinical Research SOP and Report writing

            • 1-SOP on writing a Confidentiality Agreement

            • 2-SOP on writing an investigators brochure for cli...

            • 3-SOP on the Maintenance of the study site master ...

            • 4-SOP on Procedure for drawing blood

            • 5-SOP on Measuring Vital Signs in Clinical Trials

            • 6-SOP on establishing the process for reading and ...

            • 7-SOP on Implementing the informed consent process...

            • 7-Assignment for writing an Informed Consent Form ...

            • 8-SOP on Managing source documentation

            • 9-SOP on Study Visits and Missed Visits

            • 10- SOP on Managing Study Medications

            • 11-SOP on Managing Subject Recruitment for Clinica...

            • 12-SOP on Toxicity Management, AE and SAE Reporting

            • 13-SOP on Managing subject logs and codes

            • 14-SOP on Assigning and Management of Patient and ...

            • 15-SOP on Performing Patient Screening and Enrollment

            • 16-SOP on Conducting Study Monitoring Visits

            • 17-SOP on Writing a Clinical Study Protocol (2 weeks)

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          • Cosmetics SOP and Report writing

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