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All Posts Tagged: regulatory medical writing

medical writing

Medical Writing: Answering Your Questions

1) What Is Medical Writing? Medical writing is the art of creating a document that includes medical information in a readable language which is easily comprehended by the target audience. The target audience for medical writing varies and so is the style of medical writing. Medical writing is generally divided into two categories based on purpose. One is educational medical writing while other is regulatory medical writing. Writing for layman audiences requires the use of simple words and co
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Regulatory Medical Writing

Regulatory Medical Writing: How to Manage Multiple Projects?

Regulatory Medical Writing involves writing a study protocol and/or a clinical study report (CSR) of a project. However, sometimes the medical writer has to tackle multiple projects with converging deadlines and all the study teams demanding more and more of his time. So, here are the medical writing tips to manage multiple projects efficiently. Identify the documents which are the most urgent and have the highest impact in a study. Prioritize them over those with the least impact. Ass
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Difference between Medical Writing and Science Writing

Difference between Medical Writing and Science Writing

Though the terms confuse every one, but Medical and Science writing are entirely different from each other. While Science writing deals with writing about basic science, drugs and technological innovation for the common readers, medical writing is about developing clinical and scientific documents in a standard, comprehensive, reliable and convincing manner. Here we enlist the differences between medical and science writing: 1) Medical writing demands special skills to produce well-structu
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What is Regulatory Medical Writing?

What is Regulatory Medical Writing?

Regulatory medical writing is an integral part of Medical Communications, but is often overlooked. In simple terms, it involves writing of the documents required for the approval of drugs by the regulatory authorities. The regulatory authorities like FDA, Health Canada, European Medicines Agency  and others assess the efficacy and safety of the drugs through all phases of their clinical trial and ultimately approve their use in patients. Regulatory writing helps these authorities in doing
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