Courses

  Advanced Post Graduate Diploma in Pharmacovigilance/Drug Safety (Argus Safety), Clinical Research, Clinical Data Management (Oracle Clinical) & SAS Clinical (Base SAS and Advance SAS) with Live Projects
  Advanced Post Graduate Diploma in
Regulatory Affairs
  Advanced Post Graduate Diploma in Medical Coding
 

Features

 Job Oriented Certified Training
  Live Project Experience Certification
 Placement Assistance
 Reco Letters for Abroad
  Resume Preparation Tips
  Practical Hands-on training on Databases
  Argus Safety & Oracle Clinical Databases
We are a Microsoft Dynamics Certified
Build your career in IT, CROs, Biotech & Pharma Industries

Our Candidates are
Employed with

Hands on Practical Training in Oracle Argus Safety Database (Pharmacovigilance) & Oracle Clinical OC/RDC (CDM).
For Details Fill Enquiry Form
 
Placements@:
 

You Could Become as

 
Drug Safety Associate
Pharmacovigilance Associate
Drug Safety Specialist
Aggregate Report Associate
Clinical Data Coordinator
Clinical Data Associate
Clinical Data Analyst
Clinical Data Monitor
eCRF Designer
Medical Coder
Medical Coding Specialist
Clinical Coder
Clinical Research Associate
Clinical Research Coordinator
Regulatory Affairs Associate
Healthcare Associate
SAS Programmer
SAS Developer
SAS Analyst
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WELCOME to BIOMED INFORMATICS BioMed Informatics Medwin Hospitals
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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, Medical Coding, 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.
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News & Events

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We also offer Site Management (SMO) Services for Clinical studies to Pharmaceutical, Biotechnology, CRO companies and Hospitals across a wide range of therapeutic areas. For our SMO services interested organizations can contact us.
 

BioMed in Media

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