Close. Courses in the Clinical Trials Management and Regulatory Compliance certificate use real-world clinical trials case studies to reinforce the foundational clinical trials knowledge that will accelerate your career in clinical research. What do Clinical Trials Students Learn? This modular course is designed to equip learners with specialised knowledge and expertise in the field of clinical research management, pharmaceutical regulatory affairs, pharmaceutical manufacturing and quality systems. And you’ll join a substantial network of alumni who work in the industry as you build your career. Regulatory Affairs Strategies. Regulatory affairs personnel are the first-line assurance that company products and documentation are in accordance with regulatory bodies worldwide. By the conclusion of the program, students are prepared to seek careers as clinical research coordinators, as well as clinical data managers, social science research assistants, and clinical lab techs. Over 60 courses* in the RAQA graduate program are offered online in real time. Some regulatory affairs professionals manage clinical studies or develop marketing approval policies, while others design labels for food- and drug-related products. One of the most common titles in the industry is regulatory affairs specialist. ACRP 2021 kicks off in January! Regulatory affairs and clinical development are parts of the biotech pipeline that come after discovery research and before the product can be used out in the world (which is most of that pipeline!) Get the full three-part ACRP 2021 program + 24 contact hours for just $299 through December 31, 2020. Conducting Clinical Research – Essential GCP Training for New Coordinators and Researchers E6(R2) January 2019 (3) 27-28 January, Online. I learned a lot of new and interesting things about clinical research field that I didnot know before. This course provides the clinical study sponsor strategies for working with a clinical research organization (CRO) to conduct the study. Regulatory Affairs MMHS Clinical Research Pvt. Course overview. Ltd. The regulatory function in healthcare industries is vital in making safe and effective healthcare products available worldwide. Just knowing the fundamentals of regulatory affairs is not enough to advance your career or secure a job in this industry. Regulatory Affairs course aims at entry to middle level industry professionals. in full time, part time mode with training and placement support. As DRA is an ever growing and dynamic field continuous learning and knowledge updating is the key to survival. A career in regulatory affairs can take many paths, e.g., clinical trials, drug development, food safety, medical device advancement, pharmaceutical research, or chemistry manufacturing and controls. We understand FDA requirements for clinical trials and work with global partners to ensure a shortened timeline from drug discovery to approval. In the certificate programme on Clinical Research and Regulatory Affairs, you will acquire a holistic view of these two core facets of drug development, largely through individual study, learning where and when you want. Enrolling themselves in an online course in clinical research and regulatory affairs might open new doors for them. Regulatory Affairs and Clinical Research go hand and hand, and to be a through professional, it is important for people who are looking to make a mark in this field to be well informed and trained. In this way, scientists in regulatory and clinical careers are important gateways. With lots of options, it can be intimidating to choose the right path. Ethical and Regulatory Aspects of Clinical Research. in Clinical Research, PG Diploma in Clinical Research, Clinical Trial Management, Medical Writing Course and pharmacovigilance, Clinical Data Management and Healthcare management. Ltd. Course Summary The Professional Diploma in Regulatory Affairs (PDRA) is an eLearning Program that provides a thorough understanding of the various regulatory concepts and provide expertise in the field of regulatory affairs documentation and research. Module 3 of the Global CTD. in Regulatory Affairs and Quality Assurance from the comfort of your home without ever having to commute to our campus. This comprehensive certificate program provides rigorous clinical research training across the entire clinical trials process, from the perspective of the clinical study site as well as that of the sponsor or monitor. 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