Clinical abstract application form 2026

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  1. Click ‘Get Form’ to open the clinical abstract application form in the editor.
  2. Begin by entering the particulars of the life assured. Fill in the 'Name' field, followed by the 'Identity Card / Passport No.' and 'Contract No.' to ensure accurate identification.
  3. In the Authorisation section, specify the name of the Doctor or Medical Officer-in-charge, along with their clinic or hospital details. Make sure to include the complete address for clarity.
  4. Next, provide your authorization by filling in your name and NRIC/Passport number. Clearly state that you authorize the medical report to be furnished to AVIVA LTD regarding the patient.
  5. Indicate the admission and discharge dates in their respective fields. This information is crucial for processing your request accurately.
  6. If you are 21 years old or above, sign as the patient; otherwise, have a parent or legal guardian sign on your behalf. Include their relationship to you if applicable.
  7. Finally, enter the date of signing and ensure all fields are completed before submitting your form.

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Defined as a concise summary of a medical study, research paper, or clinical presentation, medical abstracts aim to highlight the essence of a research study in a short, engaging way.
Clinical Summary a term used when the patient is still within the hospital and prior to discharge. Medical Abstract/ Discharge Summary a term used when the patient has already been discharged.
Clinical data abstraction is the process of identifying and capturing key administrative and clinical data elements. The purpose of abstraction includes the collection of data related to administrative coding functions, quality improvement, patient registry functions and clinical research.
They describe clinical trials and their results in simplified language and by way of helpful visual aids and infographics, making them easier to read and understand for people outside of the scientific community.
For most clinical research abstracts, the following areas are specifically mentioned: research design; research setting; number of patients enrolled in the study and how they were selected; a description of the intervention (if appropriate); and a listing of the outcome variables and how they were measured.

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