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Cliniminds courses
Integrated Post Graduate Diploma in Clinical Research & Pharmacovigilance - Distance learning Course
- Post Graduate Diploma
- Distance learning
- 11 Months
...In the first phase we would provide a comprehensive practical knowledge to the clinical research processes, drug development process, regulatory affairs...
- Diploma
- Distance learning
- 6 Months
...Compliance, Auditing & Quality Control in Clinical Research...
- Post Graduate Diploma
- Distance learning
- 6 Months
...investigators, clinical research professionals, other pharmaceutical industry professionals, including sales and marketing personnel and the students...
- Post Graduate Diploma
- Online
- 6 Months
...how the product is marketed on other countries, what are the legal requirements of regulatory bodies, procedure for the submission of documents...
- Post Graduate Diploma
- Distance learning
- 6 Months
...and propose and implement corrective actions. Understand the scope of failure investig The program would cover: Introduction to GMP Basic elements...
- Post Graduate Diploma
- Online
- 6 Months
...On completion of this subject students will be able to: v State the underlying principles of GMP & Quality, their significance in the industry...
- Post Graduate Diploma
- Distance learning
- 6 Months
...tests in Clinical Research. To make students aware of pitfalls in statist Biostatistics involves the theory and application of statistical science to analyze...
- Certificate
- Distance learning
- 3 Months
...Objectives Upon completion of the program, students would be able to understand the basics concept of quality assurance in clinical trials; process...
- Certificate
- Online
- 3 Months
...18 Differences between FDA and EMEA Inspections Chapter - 19 Frauds, Misconduct and Errors Chapter - 20 Practical Scenarios in Regulatory Inspections Course...
- Certificate
- Online
- 6 Months
...Recognize problems that arise with bioequivalence and generic substitution. Learn which This is a continuing training / educational program designed...
- Diploma
- Bhopal
- 6 Months
...Clinical Research Introduction - Roles & Responsibilities of Key Stakeholders - Preparations & Planning for Clinical Trials - Essential Documentation...
- Post Graduate Diploma
- Bhopal
- 6 Months
...Clinical Practices - ICH GCP General Overview of Pharmacovigilance Medical Dictionary for Drug Regulatory Activities MedDRA Regulatory Aspects in...
- Post Graduate Diploma
- Bhopal
- 12 Months
...Program Details :Healthcare Management Principles of Management Organizational Behaviour & Communication Human Resource Management Operational Research...
- Master
- Bhopal
- 2h
...This program “msc. Clinical Research & CDM” includes the following topics: * Preface of Pharmaceutical medicine * Fundamental Ethics of clinical pharmacology...
- Post Graduate Diploma
- Trichur
- 6 Months
... Clinical Research Introduction Principles of Pharmacology & Drug Discovery & Development Roles & Responsibilities of Key Stakeholders Preparations...
- Post Graduate Diploma
- Trichur
- 6 Months
...To increase the understanding of the clinical research process. Understanding of Databases & management of clinical data and SAS used in clinical trials...
- Post Graduate Diploma
- Online
- 1 Month
...Extensive Knowledge & application in different aspect s of Clinical Research The program would cover: - Clinical Research Introduction ,ICH GCP Principles & Terminology...
- Post Graduate Diploma
- Distance learning
- 11 Months
... Clinical Research Introduction Principles of Pharmacology & Drug Discovery & Development Roles & Responsibilities of Key Stakeholders Preparations...
- Post Graduate Diploma
- Online
- 6 Months
...MedDRA, case processing preparation of safety report etc. This is a continuing training / educational program designed to provide a practical knowledge for...
- Post Graduate Diploma
- Online
- 6 Months
...Development of the course involves extensive consultation with the industry. The course is suitable for health information managers, data managers...
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