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Cliniminds courses
Integrated Post Graduate Diploma in Clinical Research & Pharmacovigilance - Distance learning Course
- Post Graduate Diploma
- Distance learning
- 11 Months
...Biostatistics, Analysis & Reporting General Overview of Pharmacovigilance Medical Dictionary for Drug Regulatory Activities MedDRA Regulatory Aspects...
- Diploma
- Distance learning
- 6 Months
...designed for all the candidates aspiring to work in the field of clinical research or allied professions like central labs. The program provides complete...
- Post Graduate Diploma
- Distance learning
- 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
...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
...of a Quality Assurance program Roles of personnel working in GMP environments Facility design for cGMP compliance Concept of Clean Room Validation...
- Post Graduate Diploma
- Online
- 6 Months
...of a Quality Assurance program Roles of personnel working in GMP environments Facility design for cGMP compliance Concept of Clean Room Validation...
- Post Graduate Diploma
- Distance learning
- 6 Months
...To train students in interpretation and presentation of data collected during the conduct of a study. - To impart examples of utilisation of data in decision making...
- Certificate
- Distance learning
- 3 Months
...10 Practical Case Scenarios in Audits Module II - Regulatory Inspections Chapter - 11 FDA Inspections- Preparation, Conduct, Reporting and Recording...
- Certificate
- Online
- 3 Months
...Inspections Chapter - 12 EMEA Inspections- Preparation, Conduct, Reporting of Inspections Chapter - 13 MHRA Inspections- Preparation, Conduct...
- Certificate
- Online
- 6 Months
...New Drug Application Introduction to BA/BE and Phase-I Study Types of BE Studies Designing and Conducting BA/BE Studies Conduct & Management of BA/BE Studies...
- Diploma
- Bhopal
- 6 Months
...designed for all the candidates aspiring to work in the field of clinical research or allied professions like central labs. The program provides complete...
- Post Graduate Diploma
- Bhopal
- 6 Months
...Candidate should able to understand the. basic concepts, importance of Pharmacovigilance and Global Pharmacovigilance regulations. Practical aspects...
- Post Graduate Diploma
- Bhopal
- 12 Months
...‐ Biostatistics & Research Methodology Healthcare Marketing & Patient Relation Management Economics & Business Development Legal Aspects of Healthcare...
- Master
- Bhopal
- 2h
...vigilance * Biostatistics Outline * Preface of managing clinical information * Enterprises clinical information administration instruments * Study setting...
- Post Graduate Diploma
- Trichur
- 6 Months
...& Planning for Clinical Trials Essential Documentation in Clinical Research & Regulatory Submissions Clinical Trials Project Planning & Management...
- Post Graduate Diploma
- Trichur
- 6 Months
...Provide a known standard of professional qualification. - Facilitate the recruitment of experienced staff. - Enhance career opportunities for Clinical Data Managers...
- Post Graduate Diploma
- Online
- 1 Month
...of a candidate for the Clinical Research Associate and other key positions. Become more familiar with roles/jobs as part of the study team. Extensive Knowledge...
- Post Graduate Diploma
- Distance learning
- 11 Months
... Study Start Up Process Clinical Monitoring Essentials Compliance, Auditing & Quality Control in Clinical Research Clinical Data Management...
- Post Graduate Diploma
- Online
- 6 Months
...Clinical Practices - ICH GCP General Overview of Pharmacovigilance Medical Dictionary for Drug Regulatory Activities MedDRA Regulatory Aspects in...
- Post Graduate Diploma
- Online
- 6 Months
...To increase the understanding of the clinical research process. Understanding of Databases & management of clinical data and SAS used in clinical trials...