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Chapter 1: Introduction to Health Research: Part 5 Critical consideration on planning phase of Health Research Basic Course in Biomedical Research Tutorials by Dr. Tanmay Mehta Basic course in Biomedical Research Question bank https://qworld.co.in/product/1152/basic-course-in-biomedical-research-question-bank It is online question bank which covers…
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Chapter 1: Introduction to Health Research: Part 4 Study designs in Health Research Basic Course in Biomedical Research Tutorials by Dr. Tanmay Mehta Basic course in Biomedical Research Question bank https://qworld.co.in/product/1152/basic-course-in-biomedical-research-question-bank It is online question bank which covers 650+ Multiple choice quest…
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Chapter 1: Introduction to Health Research: Part 3 Process, Study variables and Scope (Objectives) of Health Research Basic Course in Biomedical Research Tutorials by Dr. Tanmay Mehta Basic course in Biomedical Research Question bank https://qworld.co.in/product/1152/basic-course-in-biomedical-research-question-bank It is online question bank which…
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Basic Course in Biomedical Research Tutorials by Dr. Tanmay Mehta Chapter 1: Introduction to Health Research: Part 2 Principles of Health Research Basic course in Biomedical Research Question bank https://qworld.co.in/product/1152/basic-course-in-biomedical-research-question-bank It is online question bank which covers 650+ Multiple choice question…
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Basic Course in Biomedical Research: Chapter 1: Introduction to Health Research: Part 1 Dimensions of Health Research Basic Course in Biomedical Research Tutorials by Dr. Tanmay Mehta Basic course in Biomedical Research Question bank https://qworld.co.in/product/1152/basic-course-in-biomedical-research-question-bank It is online question bank which…
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Basic Course in Biomedical Research Tutorials by Dr. Tanmay Mehta Basic course in Biomedical Research Question bank https://qworld.co.in/product/1152/basic-course-in-biomedical-research-question-bank It is online question bank which covers 650+ Multiple choice questions (MCQs) in exam mode and practice mode for the final exam of the Basic course in…
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It is mandatory to follow the Good Clinical Practice (GCP) rules for trials involving drugs. This episode will give you the background and the main content of the GCP regulations and what it practically means to you when running the study. It is no way a full description of the GCP concept but will give you the highlights so that you can find furth…
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You do not need to be an expert in the clinical field to write a systematic review. It is a fairly easy process because it follows a specific guideline (the PRISMA guideline), and it is also fairly easy to get it accepted for publication in a journal if you do it the right way. And importantly, you will automatically read the necessary literature i…
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Before study start (meaning before accrual of the first patient) you have to obtain certain permissions and perform certain registrations. There are differences from country to country but you will always need ethical committee approval for a clinical trial.
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The best way to get the idea for a research project is to listen to the questions asked by the patient and by younger colleagues and medical students. They often ask the relevant questions, and these can very easily be translated into research questions.
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Everybody needs a mentor. When you look for a mentor the most important factor is chemistry. You will spend a lot of time together with your mentor so communication has to be pleasant and productive. The research area may not be that important as long as your mentor is the right person for you.
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The submission proces has certain steps and include the manuscript system used by the journal, a cover letter, submission of different files, and if you get a chance to revise your paper, the revised paper should be submitted with a detailed rebuttal letter.
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There are different issues to consider when you are deciding for a target journal for your scientific article. The best advice is to decide as early as possible because it may influence the writing of the paper and even the study design in some cases.
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The narrative review may be a difficult article to write for the novice science writer. The reason is that it does not follow explicit rules or guidelines. There are a few tricks, however, so listen to the podcast and learn how to build your next narrative review.
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It may be important and a very good idea to publish a protocol article with its statistical analysis plan before enrolment of patients in the study. This will secure the analysis plan and ensure that the researchers will not go on a fishing expedition in tha data analysis phase. In the episode we discuss how to build the protocol article.…
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You may not realize how important this is, but your image as a researcher is actually reflected in your reference list. If you make errors in the reference list, then the editor and peer reviewers may suspect that you have also made errors in the research project itself. So be careful and correct all errors in the reference list. It has to be absol…
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In the biomedical sciences we use the ICMJE criteria for authorship, and if these are followed there is actually no upper limit for the number of authors on a scientific paper as long as all authors fulfill the four authorship criteria.
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There has been a tendency, especially in larger trials, to use a group name in the author byline. With the current clear definitions of authorship the use of a group name in the byline may be a little old-fashioned. The episode will discuss the pros and cons of using a group name, and will guide you to have your group name indexed even without usin…
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When you want to refer to a specific webpage in your reference list then there is a risk that the webpage will not be available forever. You can therefore use a smart trick to ensure that your referred webpage will always be available for the reader. This is explained in this weeks episode.
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In this issue we discuss various issues of trial registration, including where to register, what to register, and how to find registered studies with a search covering all the available databases. All trials should be registered and the term "trial" typically covers interventional human clinical trials. There may, however, be good reasons also to r…
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