Clinical Data Management (CDM) is a division of Healthcare science that determines the protection and effectiveness (efficacy) of the medications, procedure, diagnostic products and treatment regimens anticipated for human use. These may be used for anticipation treatment diagnosis or for relieving symptoms of infection. Clinical Data Management is one of part in Clinical research practice. In clinical research data is collected to start a treatment. The term clinical research refers to the entire case study of a medicine/appliance/biologic, in fact, any test piece from its setting up in the lab to its prologue to the consumer market and beyond. In addition referred to as Clinical trial management are attractive industries which foresee remarkable growth and employment opportunities for qualified medical, pharmaceutical, paramedical professionals and Life Science Graduates. With the inflow of worldwide players in research, the industry is on the edge to grow exponentially and open up new vistas of employment for a great number of people.
Medical writing (MW) is a area that has gained energy over the last few years. Medical and scientific writing involves writing manuscripts which are necessary by the medical / scientific organization and the pharmacy-biotech profile including clinical research & clinical data management. The main two key domains in the pharmaceutical and biotechnology segment where medical writers are in sky-scraping demand are pharmaceutical regulatory writing and promotional material writing i.e. Medico-marketing writing for the drug manufacturing industry. The main responsibility of medical writers is to generate well written documents and manuscripts as per regular formats, submissive to regulatory standards for endorsement of new clinical trials, drugs, medical procedure and biologics.