Cliniminds is an innovative clinical research training institute providing a wide
range of clinical trials training solutions to the students, pharmaceutical companies,
CROs and healthcare companies globally.
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. Company was set up with the objective to offer education
and training solutions in the field of clinical research, pharmaceuticals and healthcare.
Cliniminds today is one of the best clinical research training institutes. Cliniminds
clinical research 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, USA, Mexico, U.K., Canada, Europe, Africa, Asia
and Middle East. Cliniminds today is the leader in the clinical research education
and training domain. Today Cliniminds is being rated amongst the best quality clinical
research institutes globally.
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. 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 clinical trials, or
update your knowledge with current information.
- Courses Offered through Classroom; Online; Distance Learning & E-Learning.
- User-friendly Online Learning System.
- State-of-the-art Learning Management System.
- High Quality Course Content.
- Cost Effective.
- Professional Faculty.
- Programs cover wide variety of clinical trials issues, viz. ICH GCP Principles;
Regulatory affairs; clinical trial documentation; ethics; monitoring; project management;
roles & responsibilities; quality assurance; audits & inspections; introduction
to pharmacology; pharmacovigilance; bio equivalence & bio availability studies;
data management; bio statistics; SAS; European, USFDA Schedule Y and other regulations;
medical & scientific writing; investigator training, CRA/CRC training and several
other trial issues.
- Convenient 24x7 format using Learning Management System.
- Targeted Programs.
- Placement Support.