POST GRADUATE DIPLOMA IN DRUG REGULATORY AFFAIRS, IPR & PATENT
FULL TIME PROGRAM – 6 MONTHS + 3 MONTHS INTERNSHIP : 100% PLACEMENT SUPPORT : INDUSTRY CERTIFICATION :ADD ON SPECIALIZATION IN PHARMACOVIGILANCE
LOCATION-DELHI
WELL PROGRAM : WORK, EARN, LEARN & LEAP
ADVANCE POST GRADUATE DIPLOMA IN CLINICAL RESEARCH & PHARMACOVIGILANCE
WEEKEND PROGRAM – 6 MONTHS : 100% PLACEMENT SUPPORT : INTERNSHIPS : INDUSTRY CERTIFICATION : ADD ON CLASSES IN MEDICAL & SCIENTIFIC CONTENT WRITING
LOCATION-DELHI
WELL PROGRAM : WORK, EARN, LEARN & LEAP
ADVANCE POST GRADUATE DIPLOMA IN CLINICAL RESEARCH, CLINICAL DATA MANAGEMENT & SAS
FULLTIME PROGRAM – 6 MONTHS : 100% PLACEMENT SUPPORT : INTERNSHIPS : INDUSTRY CERTIFICATION : DUAL CERTIFICATION
LOCATION-DELHI
WELL PROGRAM : WORK, EARN, LEARN & LEAP
Inside Cliniminds
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Cliniminds was established in year 2004, by a group of professionals from Clinical Research, Pharmaceutical industry and Healthcare industry with rich and varied experience at senior management levels.
Cliniminds offers Educational & Training Programs to develop the skill capacity in the health sciences domain. Cliniminds is an innovative health sciences educational and training institute providing a wide range of clinical trials, regulatory, phamracovigilance, data management and other job oriented training programs. We also provide training and continuing medical education solutions to the, pharmaceutical companies, CROs, hospitals, and healthcare companies globally.
Cliniminds programs enjoy very high level of acceptance from leading global pharmaceutical and clinical research companies. Cliniminds Online Programs are popular amongst the students from India, United States of America, Mexico, U.K., Canada, Europe, Africa, Asia and Middle East. Cliniminds today is the global leader in the clinical research and pharmacovigilance education and training domain. Cliniminds is rated amongst the best quality clinical research institutes globally. Cliniminds has been awarded as the Best Clinical Research Institute in India consecutively for two years – 2011 & 2012.
Good Clinical Practice (GCP) guidelines and regulations of respective countries govern conduct of clinical trials, and a thorough knowledge of procedures at every stage of the clinical trial process is essential. Our programs also cover wide variety of clinical trials, pharma and health sciences issues, viz. ICH GCP Principles; regulatory affairs; clinical trial documentation; ethics; monitoring; project management; roles & responsibilities; quality assurance; audits & inspections; pharmacology; pharmacovigilance; drug safety; bio equivalence & bio availability studies; clinical data management; bio statistics; SAS; European, USFDA, EMA Schedule Y and other regulations; medical & scientific writing; investigator training, CRA/CRC training and several other trial issues.
Cliniminds 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 health sciences domain, update your knowledge with current information.
MAIN FEATURES OF THE PROGRAMS
  • Job Oriented with placement focus.
  • Curriculum designed in collaboration with the industry.
  • Programs offered through full time, weekend; online; distance learning & e-learning / video conferencing mode.
  • User-friendly online learning system with state-of-the-art learning management system.
  • Industry experienced professional faculty.
  • Wide range of programs.
  • High quality course content.
  • Cost affective & affordable programs.
  • Convenient 24x7 format using Learning Management System.
  • Industry targeted programs.
  • Active placement support.
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Dr. Subodh Bhardwaj
MD (Pharmacology) – Director of Health Sciences Education & Training
A innovative Medical Doctor with post - graduation in Pharmacology and more than 30+ years of experience in
Clinical Medicine, Clinical Research, Pharmacovigilance and Drug Regulatory Affairs.Read More...