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26.8.11
CLINICAL RESEARCH
CLINICAL RESEARCH
CLINI INDIA brings you an opportunity to be a part of a emerging Industry of CR, provided by industry leaders. By this training you will be able to explore a plethora of opportunities in the emerging Industry. Get set to explore new dimensions and draw helpful insights from 27th Aug to 5th Sep 2011 at CLINI INDIA campus.
Admission open for-
Advanced Program in Clinical Research & Management.
Starting From- 1st Sep 2011
Admission Last date: 31th Aug 2011
Program Covers all the following Module.
• CLINICAL TRIAL OPERATIONS |
• CLINICAL DATA MANAGEMENT |
• PHARMACOVIGILANCE |
• MEDICAL WRITING |
• REGULATORY AFFAIRS
Duration: 3 months(Classroom) + 1 month (Internship)
Why Choose CLINI INDIA-
• 100% Industry Visiting Faculty
• One Month Industry Internship
• Industry Endorsed Curriculum
• Soft Skills Training
• Hands On Training on CDM
• Complimentary Study material Books, Pen drive etc.
• Pre-Placement training
• Mock Interviews
CLINI INDIA is a Premier Clinical Research Training Institute, offering Training in Clinical Research, Clinical Data Management, Pharmacovigilance and medical Writing.
Name:_____________________
Qualification:________________
Phone No:__________________
City:______________________
For More Info and appointment call 040- 65550643, 07799400500
Visit www.cliniindia.com & be a part of our upcoming boom In healthcare.
10.3.11
Pharmacovigilance is a new discipline to the students of India which provides newer and better opportunities to aspirants across the country who wish to build their career in the field of pharmacological science.
Pharmacovigilance is a discipline which is concerned with identifying, validating, quantifying, evaluating and minimizing the adverse effects of medicine thereby increasing the safety of drugs in use. It is a study of drug related adverse effect carried out by pharmaceutical industries to suggest warnings and recommendation for product withdrawal.
Pharmacovigilance is not only an academic necessity but also a need to ensure security of human beings. It is an accepted opinion of the mass to scrutinize the adverse effects of medicines which have been released in the market.
The Government also puts forward a supportive hand and takes immediate actions for the implementation of such a course so that people become aware of the adverse effects of drugs which can be reduced by a discipline like pharmacovigilance.
Pharmacovigilance is important to implement quality systems in all pharmaceutical companies which produce huge amount of medicines that are marketed in India and Western Countries.
Courses
An aspirant of pharmacovigilance can pursue both certificate and diploma courses in pharmacovigilance.
The certificate course for Pharmacovigilance and Pharmacoepidemiology is for 4 months. The course is conducted by CLINI INDIA. The course fee is Rs.50,000 - Rs.80,000.
The two courses are taught by expert international faculty and well known national faculty who have several years of pharmacovigilance experience in practical and theoretical field.
To participate in these programmes of Pharmacovigilance, the eligibilities are:
Graduates in Pharmacy and Bio-Sciences, Medical Professionals, i.e Doctors of all disciplines, graduates in pharmacy and bio-sciences and junior professionals in Pharmaceutical and IT Industry, Clinical Research Organization are eligible for the course.
7.1.11
CLINI INDIA-CAMPUS
ABOUT CLINICAL RESEARCH
Clinical research is a growing, Multi-billion dollar industry that provides a unique, Challenging truly global and lucrative career options.
The worldwide demand for clinical research is so vast that India , with its booming economy, skilled manpower and thick populace, is considered as a leading player in the arena of clinical research. India represents an upcoming global hub for clinical research industry.
It is estimated that clinical research industry in India will touch Rs. 7000 crores by 2010** and the industry will employ more than 50,000* professionals in India and 2,50,000* globally in the next 5 years. This would comprise jobs in various fields such as clinical operations, data management, medical and regulatory writing, pharmaco-vigilance, quality assurance and managerial positions.
*McKinsey Report **CII Report
PROGRAM FEATURES:
INDUSTRY ENDORSED COURSE CURRICULUM
Clinical Trial Management
Clinical Data Management
Pharmacovigilance
Medical Writing
SOFT SKILLS TRAINING:
Communication Skills Development
Behavioural Skills
Corporate Communication
Interviewing Skills
Resume /covering letter designing
FACULTY:
Industry Faculty from leading organizations conducting Clinical Trial.
100% Visiting Faculty from Industries
Industry Designed Course Syllabus
Case Studies based on live Projects
STUDY MATERIAL:
Institute will provide Required Study material, Pen drive, Printouts and Soft copy of the Presentation slides etc.
INTERNSHIP:
Institute will assist you to provide an internship.
PLACEMENT:
Placement Support by the Institute.
Pre-placement assistance
Alumni- Student Support for placement.
Resume /Covering letter designing.
CLINICAL RESEARCH INSTITUTE
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Clinical Data Management
PCCRCDM (Professional Certificate In Clinical Research And Clinical Data Management)
Course Content:
Clinical Trial Process
Clinical Trial Design
Ethics & Good Clinical Practice
Clinical Data Management
CRF Design
Data Entry
Data Collection
Data Load
Data Storage
Data Validation
Query Management
Data Archiving
Quality Systems, Sops & Audits
Regulatory Affairs & Compliance
Safety Management and Pharmacovigilance
Statistical Analysis & Reporting
Data Management Systems & Tools
CDMS
AERS
EDC
Analytical Tools
Documentation & Document Management System
Medical coding and medical dictionaries
Project Management
Security systems
Practical:
Clinical Data Management System
Study Set-Up
Database Creation
CRF Creation
Data Entry
Data Validations
Query Management
Database lock
Statistical Software