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Clinical Trials (Medical Devices Trials) Regulations 2021 GN No. 100 of 2021 Government Gazette of Mauritius No. 56 of 7 May 2021THE CLINICAL TRIALS Autoregulations made by the Minister under section
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How to fill out long-term follow-up study of

01
Step 1: Gather all necessary information such as patient demographics, treatment information, and follow-up schedules.
02
Step 2: Ensure proper documentation of patient consent for participation in the long-term follow-up study.
03
Step 3: Use standardized forms and databases to record and track follow-up data over the designated period of time.
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Step 4: Monitor and address any potential challenges or barriers to successful follow-up participation.
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Step 5: Analyze and report on the collected data to assess the long-term outcomes of the study participants.

Who needs long-term follow-up study of?

01
Patients who have participated in clinical trials or received specialized medical treatment that may have long-term effects.
02
Researchers and healthcare professionals interested in studying the ongoing impacts of specific interventions or therapies.
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Regulatory agencies and policymakers looking to evaluate the safety and efficacy of new treatments over an extended period of time.
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Long-term follow-up study is a research method that follows participants over an extended period of time to assess outcomes.
Researchers conducting long-term follow-up studies are required to file the study.
Long-term follow-up study is typically filled out by collecting data on participants at specific intervals over a long period of time.
The purpose of long-term follow-up study is to track the health and well-being of participants over an extended period of time.
Information reported on long-term follow-up studies may include demographics, medical history, treatment received, and outcomes.
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