Online Training in Clinical Research & Regulatory Affairs :-As a specialist in clinical research and regulatory affairs, you serve in a pharmaceutical company or a public health sector, bearing responsibility for documenting and authenticate the quality, efficacy and safety of drugs in approval applications for regulatory. You evaluate and document the compliance of clinical studies to regulatory needs. You issue relatable specifications for the scheduling, implementation and estimation of clinical studies to the division concerned. You use the outcomes of such studies in the clinical study report, the approval dossier, the medical records and the patient information brochure. You identify potential risks for the approval of a drug early on and can interfere if necessary.
The Online Training in Clinical Research & Regulatory Affairs educates you the parameters, techniques and procedures of clinical research, and of novel drug approval in the European and American markets. The program emphasizes on the interfaces and interdependencies between clinical research and drug approval processes.
James Lind Institute’s Online Training in Clinical Research & Regulatory Affairs Program offers you with exhaustive training on present regulations and their real world application to the development and commercialization of biotechnology, pharmaceutical, medical device, and healthcare related products.
James Lind Institute offers Online Training in Clinical Research & Regulatory Affairs. If you wish to enroll Clinical Research & Regulatory Affairs Training please apply now.