Cliniminds India - Invidious

Cliniminds India

Cliniminds was established in Year 2004 – Tenet Health Edutech Pvt. Ltd., promoted by team of Industry professionals and academia. Its India’s first skill development institution in life sciences domain to receive Pharmaceutical Society of India (PSI), Accreditation Council for Clinical Research Education (ACCRE U.S.).

Following courses we offer; Advanced Post Graduate Diploma in Pharmacovigilance, Data Management & SAS, Advanced Post Graduate Diploma in Pharmacovigilance & Medical Writing, Post Graduate Diploma in Medical & Scientific Content Writing, Advanced Post Graduate Diploma in Pharmacovigilance.

We offer wide range of skill development clinical research, pharmaceutical and healthcare educational programs and training solutions
Our programs sustained by superior copyright content and faculty with global stand point.
We have national Presence – 15 major cities in India, International Centers: USA ; UK, RUSSIA and UAE
For more information contact : elearn@cliniminds.com

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4:07

Cliniminds Literature search - Pharmacovigilance

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3:07

Cliniminds Aggregate Report Writing Program - PSUR Writing (Periodic Safety Update Reports)

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18:46

Cliniminds Orientation August 2025 - Drug Regulatory Affairs, IPR & Patents

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3:53

Feedback given by Dr Richa Kumari - Cliniminds Student

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1:03:36

Cliniminds Orientation July 2025 - Clinical Research, Pharmacovigilance, Clinical Data Management

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4:42

International Council for Harmonisation (ICH)

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4:17

Pharmacovigilance Programme of India (PvPI)

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3:56

Common Technical Documents - Drug Regulatory Affairs

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3:05

Naranjo Scale - Pharmacovigilance

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3:26

Data Management Plan (DMP) - Clinical Data Management

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3:00

Database Lock Point - Clinical Data Management

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2:46

Principal of ALCOA+ in Clinical Data Management

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1:02

When did the formal celebration of Clinical Trials Day begin?

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2:48

User Acceptant Testing - Clinical Data Management

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2:46

Clinical Trial Agreement (CTA) - Clinical Research

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3:37

Introduction of PBRER (Periodic Benefit-Risk Evaluation Report) - Aggregate Report Writing

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5:30

Introduction of Aggregate Report

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184 views

4:45

eCRF Completion Guidelines

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0:29

New Beginnings, Bright Futures: Celebrating Devesh Aggarwal’s Success

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2:52

Audits and inspection in Clinical Research

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7:35

Why 'Results' Are the Heart of Medical Writing

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2:55

Clinical Research| where clinical trials take place?

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3:09

The Importance of Probing in Adverse Events

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8:20

Medical Device Regulation - Regulatory Affairs

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240 views

8:46

Orientation Session of Pharmaceutical Business Analytics - 23rd March 2025

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112 views

8:40

Chemistry, Manufacturing, and Controls (CMC) - Drug Regulatory Affairs

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196 views

6:56

eCTD Software Training – Drug Regulatory Affairs

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1.3K views

5:48

Hands-on Training on PBRER ( Periodic Benefic Risk Evaluation Report )

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258 views

7:32

Aggregate reports (PSUR)

Cliniminds India

Shared 6 months ago

264 views

4:51

Overview of Healthcare Systems in United States - Healthcare Analytics

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556 views

7:43

Epidemiology - PHARMACEUTICAL BUSINESS ANALYTICS

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94 views

6:05

Importance & Composition of Ethics Committee

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224 views

19:58

Health Technology Assessment (HTA) in Europe - HEOR

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136 views

6:52

Investigator and Site Selection - Monitoring of Clinical Trials

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163 views

5:44

The Role of Regulatory Authority in Clinical Trials PPT Presentation By Shriya Kesherwani

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8:32

Responsibilities of Ethics Committee- PPT Presentation By Anjali Bachulkar

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144 views

4:19

Clinical Trial Registries -PPT Presentation By Keerthi S

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126 views

8:06

Phases of Clinical Trials - PPT Presentation By Dr. Reshma Madaan

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350 views

7:12

Phase 3 Clinical Trial PPT Presentation By Anvita Gangan

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209 views

4:14

PADER Report (Periodic Adverse Drug Experience Report)

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Shared 7 months ago

368 views

8:30

Computer System Validation (CSV)

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780 views

5:59

The Republic Day celebration by Cliniminds Students and Teachers

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Shared 7 months ago

60 views

6:57

Creation of Data Transfer documents - Clinical Data Management

Cliniminds India

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253 views

21:18

Emerging Global Trends in Pharmaceutical Regulatory Affairs

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190 views

5:27

Importance of External Data - Clinical Data Management

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203 views

11:01

Regulatory framework in the European Union - Drug Regulatory Affairs

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608 views

6:45

Drug Master File - Regulatory Affairs

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Shared 7 months ago

202 views

9:09

Systematic Literature Reviews - PICOTS Criteria -Health Economics & Outcomes Research (HEOR)

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Shared 7 months ago

172 views

17:31

Introduction of SAS ( Statistical Analysis System)

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Shared 8 months ago

434 views

3:58

Signal Management process

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194 views

2:05

Serious Adverse Drug Reaction process

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133 views

2:01

Investigational New Drug (IND)

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Shared 8 months ago

129 views

12:46

Regulatory writing / Medical Writing - CMC Module

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519 views

10:17

New drugs and clinical trial (NDCT) rules 2019

Cliniminds India

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1.1K views

19:17

Council for International Organizations of Medical Sciences (CIOMS)-Good Pharmacovigilance Practices

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316 views

13:56

Regulatory Framework in Latin America - Drug Regulatory Affairs

Cliniminds India

Shared 8 months ago

181 views

9:31

MedDRA (Medical Dictionary For Regulatory Activities) – Pharmacovigilance

Cliniminds India

Shared 9 months ago

529 views

7:30

Regulatory Filing System in USA - Drug Regulatory Affairs

Cliniminds India

Shared 9 months ago

217 views

16:43

Clinical Data Management Software Training

Cliniminds India

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1.1K views

15:45

Phase1 Study in clinical research

Cliniminds India

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148 views