BioMed Informatics Medwin Hospitals was set up as a premier research centre with the objective to offer services in the field of Pharmacovigilance, Clinical Research, Clinical Data Management (CDM), SAS Clinical, Oracle Argus Safety Database, Oracle Clinical OC/RDC, Intellectual Property Rights-IPR, Regulatory Affairs and Healthcare since the year of 2000.
BioMed Informatics today is one of the best Pharmacovigilance, Clinical Research and Clinical Data Management (CDM) training institutes. BioMed Informatics programs enjoy very high level of acceptance from leading global Pharmaceutical, Biotechnology, CROs and Clinical Research companies. BioMed Informatics Programs are popular amongst the students from India, USA, Mexico, U.K., Australia, Canada, Europe, Africa, Asia and Middle East. BioMed Informatics today is the leader in the Pharmacovigilance, Clinical Research and Clinical Data Management (CDM) education and training domain.
Good Clinical Practice (GCP) regulations and guidelines govern Clinical Trials, and a thorough knowledge of procedures at every stage of the Clinical Trial process is essential. BioMed Informatics can help you achieve the level of expertise required through our high quality, user-friendly and cost-effective training programs - whether you need to train for a career in Clinical Trials, or update your knowledge with current information.
BioMed Informatics Medwin Hospitals imparting quality Career Oriented Certified Training Programs in Pharmacovigilance, Drug Development Process, Clinical Research, US FDA Regulatory Affairs, Clinical Data Management (CDM), Clinical SAS, Oracle Argus Safety Database, Oracle Clinical OC/RDC with live project implementation and certification.
We also offer Site Management (SMO) Services for Clinical studies to Pharmaceutical, Biotechnology, CRO Companies and Hospitals across a wide range of therapeutic areas.