Cliniminds has set up a Representative Office in Czech Republic to provide Online
Clinical Research Educational & Training Programs to the students from Czech Republic,
Slovakia, Poland, Hungary, Russia, Kazakhstan, Ukraine, Lithuania, Latvia, Estonia,
Turkey, Romania and Bulgaria. Cliniminds Online Learning System is highly user friendly
with very high quality training content for all the programs. All programs are conducted
in English.
- Programs designed keeping in view needs of the international students
- No English Evaluation Requirement
- The academy has ISO certification. Our Programs are accredited and certified by
the Pharmaceutical Society of India. Cliniminds is member of DIA and NIH. Cliniminds
programs are used by the major multinational companies and organisations like Merck
and NIH.
- Efficient Student Query Response System
- User friendly Learning Management System
- High Quality Content
- Affordable Costs
- 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