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Comprehensive practical knowledge to the clinical research process, drug development process, regulatory affairs, essential documentation, roles and responsibilities, ethics, monitoring, conduct and management of trials, extensive training on Clinical Research and Data Management related issues.
Module 1 | Clinical Research Introduction |
Module 2 | Principles of Pharmacology & Drug Discovery & Development |
Module 3 | Roles & Responsibilities of Key Stakeholders |
Module 4 | Preparations & Planning for Clinical Trials |
Module 5 | Essential Documentation in Clinical Research & Regulatory Submissions |
Module 6 | Clinical Trials Project Planning & Management |
Module 7 | Study Start Up Process |
Module 8 | Clinical Monitoring Essentials |
Module 9 | Compliance, Auditing & Quality Control in Clinical Research |
Module 10 | Overview of Clinical Data Management & Biostatistics |
Hands on training on software, online live classes/classroom
Online MCQs/Classroom
Post Graduate Diploma would be awarded upon successful completion of the program. Program accredited by Accreditation Council for Clinical Research Education, USA.
Training would be imparted by the fulltime Think I & Cliniminds faculty and visiting experts from the industry.
Life Long
Face to Face {3 Months Full time Classroom+ 03 Months Optional Industry Internship, 6 Months Weekend (Saturday/Sunday) no internship for weekend batch}
E learning {6 Months without internship)
Distance Learning {6 months}
Please contact counsellor for upcoming batch details 91 812 910 0876 / 91 484 421 6666 / 1800 1023 566 (Toll Free)
COURSE FEE
Actual Fee 110000+18% GST
*Inclusive of applicable tax
MD, MS, MBBS, BDS, BHMS, BAMS, BUMS, BPT, B. Pharm, Graduate/Post Graduate Degree in Life Sciences, Mathematics, Pharmacology, Pharmacy, Medical Laboratory, Nursing, Biochemistry, Microbiology, Biotechnology, and all professionals working with Pharmaceutical companies, Clinical Research Organisations and Hospitals.
TOLL FREE : 1800 102 3566