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University M.Sc. Program
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Course Name
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Duration
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Masters(M.Sc.) in Clinical Research & Clinical Data Management(MCRD)*
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24 Months
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Course Information
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Admissions Ongoing
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Registration Form
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Live Interactive Video Conferencing Classes : Sunday Classes(Batch commences-Mid June 2010)
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Course Name
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Duration
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Advanced Post Graduate Diploma in Pharmacovigilance
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6 Months
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Course Information
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Advanced Post Graduate Diploma in Regulatory Affairs,Intellectual Property Rights & Patents
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6 Months
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Course Information
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Admissions Ongoing
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Registration Form
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Cliniminds Programs
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Course Name
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Duration
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University Diploma Programs
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Course Name
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Duration
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Post Graduate Diploma in Clinical Research & Clinical Data Management(PCRD)
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12 Months
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Course Information
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Post Graduate Diploma in Clinical Research & Pharmacovigilance(PCRP)
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12 Months
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Course Information
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Post Graduate Diploma in Clinical Research & Regulatory Affairs(PGDCRA)
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12 Months
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Course Information
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Post Graduate Diploma in Clinical Trials Management(PCTM)
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12 Months
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Course Information
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Post Graduate Diploma in Pharmacovigilance(PDPV)
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12 Months
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Course Information
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Admissions Ongoing
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Registration Form
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Limited scholarships available.Send cv to hyderabad@cliniminds.com
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For more information contact
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Mob: +91-9666686966,9311168241
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Tel : +91-040-66736966
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Cliniminds has set up a Branch Office in Hyderabad and a company owned centre Cliniminds
would be offering wide range of programs at Hyderabad centre Hyderabad centre would
cater to the students from entire Andhra Pradesh Programs would be offered through
various modes viz Classroom, Online/Distance Learning and E-Learning (Videoconferencing)
based classrooms.
- Advanced Post Graduate Diploma in Clinical Research & Pharmacovigilance
- Advanced Post Graduate Diploma in Biostatistics & SAS
- Advanced Post Graduate Diploma in Clinical Data Management, Biostatistics & SAS
- Advanced Post Graduate Diploma in Clinical Research & Regulatory Affairs in Pharma & C R
- Advanced Post Graduate Diploma in Clinical Research
- Diploma in Clinical Research
- Post Graduate Diploma in Pharmacovigilance
- Certificate Program in Conducting & Managing Bioequivalence & Bioavailability Studies
- Certificate Program in Conducting & Managing Clinical Trials for Cancer Patients
- Certificate Program For Clinical Trial Investigators & Site Personnel
- Certificate Program in Monitoring of Clinical Trials
- Post Graduate Diploma in Clinical Trials Management
- Post Graduate Diploma in Clinical Research for Nurses
- Certificate Program in Quality Assurance in Clinical Research
- Post Graduate Diploma in Regulatory Affairs
- ICH GCP Certificate Program In Clinical Research For Medical Practitioners
- Post Graduate Diploma in Medical and Scientific Content Writing
- Post Graduate Diploma in cGMP – Good Manufacturing Practices
- Certificate Program in Clinical Trial Regulations & GCP in Europe & UK
- Certificate Program in Clinical Trials Auditing & Inspection
- Advanced Post Graduate Diploma in Clinical Data Management
- Advanced Post Graduate Diploma in Clinical Research & Bioequivalence & Bioavailability Studies
- Advanced Post Graduate Diploma in Regulatory Affairs ,Intellectual Property Rights and Patents
- Post Graduate Diploma in Clinical Research for Medical Devices
- Integrated Post Graduate Diploma In Clinical Research & Pharmacovigilance
- Post Graduate Diploma in Clinical Data Management & SAS
- Post Graduate Diploma in Clinical Trials Quality Assurance, Auditing & Inspections
- Post Graduate Diploma in Intellectual Property Rights & Patents