HOW TO BECOME A COMPETENT MEDICAL WRITER?

Medical writing Service is a specialized area of writing where the medical writer needs to develop different types of scientific documents that include research related documents in the field of medical science and associated regulatory areas. The demand for competent, professional medical writers is growing at a rapid pace due to an exponential growth of pharmaceutical companies, diagnostic field and health care related portals, which require effective health care communication materials to promote their medicines, medical devices, related products and services to the doctors, patients and the general public.

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WRITING MEDICAL CONTENT FOR CLINICAL RESEARCH-QUICK GUIDE FOR CLINICAL PRACTITIONERS AND RESEARCHERS

Medical content Writing is an integral component of clinical research that is essential for effectively taking research related scientific communications to the target audience like medical specialists and health care professionals. Effective and well-structured medical contents with appropriate research design and reference support is imperative for every aspiring medical researcher to publish their clinical research studies in reputed national and international medical journals. Click Here to know more...

WRITING GRANT PROPOSALS FOR PHARMA RESEARCH/CLINICAL STUDY

Grant writing is a skill of critical significance to the global pharmaceutical industries and clinical research professionals, as conducting high-quality clinical research studies needs large amounts of funds, which can be obtained by writing successful grant proposals Click Here to know more

WRITING A BIOLOGICAL SAFETY ASSESSMENT (BSA) REPORT: PREMARKETING REQUIREMENT RISK ASSESSMENT

Biological Safety Assessment or BSA as it is called is an important and wide field. As new breakthroughs by way of medicine, crop, biotechnology increase, the need to assess the safety of medical devices becomes paramount. It provides some amount of reassurance to patients in a clinical investigation. A report should be based on medical devices directives -MEDDV 2.7.1 and clinical investigations guidelines ISO 14155. Writing a Biological Safety Assessment (BSA) report can run as under: 1 Clinical data and Evaluation and Evidence : The safety and/or performance information that is generated from the clinical use of a device and a procedure to collect, appraise and analyse clinical data pertaining to a medical device and to evaluate whether there is sufficient clinical evidence to confirm compliance with relevant essential requirements for safety and performance when using the device and an evaluation report pertaining ...

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