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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3:37

Cliniminds Dossier preparation and submissions: Drug Regulatory Affairs

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4:14

Career Opportunities in Drug Regulatory Affairs & IPR

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3:05

CLINIMINDS CASE REPORT FORMS - CLINICAL RESEARCH

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4:02

Cliniminds Protocol Design - Clinical Research

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Cliniminds CTD (Common Technical Document ) Module 1

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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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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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256 views

8:46

Orientation Session of Pharmaceutical Business Analytics - 23rd March 2025

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Shared 6 months ago

114 views

8:40

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

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209 views

6:56

eCTD Software Training – Drug Regulatory Affairs

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5:48

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

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277 views

7:32

Aggregate reports (PSUR)

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4:51

Overview of Healthcare Systems in United States - Healthcare Analytics

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7:43

Epidemiology - PHARMACEUTICAL BUSINESS ANALYTICS

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Importance & Composition of Ethics Committee

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231 views

19:58

Health Technology Assessment (HTA) in Europe - HEOR

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153 views

6:52

Investigator and Site Selection - Monitoring of Clinical Trials

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174 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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4:19

Clinical Trial Registries -PPT Presentation By Keerthi S

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131 views

8:06

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

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7:12

Phase 3 Clinical Trial PPT Presentation By Anvita Gangan

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4:14

PADER Report (Periodic Adverse Drug Experience Report)

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402 views

8:30

Computer System Validation (CSV)

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895 views

5:59

The Republic Day celebration by Cliniminds Students and Teachers

Cliniminds India

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6:57

Creation of Data Transfer documents - Clinical Data Management

Cliniminds India

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273 views

21:18

Emerging Global Trends in Pharmaceutical Regulatory Affairs

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197 views

5:27

Importance of External Data - Clinical Data Management

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228 views

11:01

Regulatory framework in the European Union - Drug Regulatory Affairs

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6:45

Drug Master File - Regulatory Affairs

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Shared 8 months ago

212 views

9:09

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

Cliniminds India

Shared 9 months ago

177 views

17:31

Introduction of SAS ( Statistical Analysis System)

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456 views

3:58

Signal Management process

Cliniminds India

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200 views

2:05

Serious Adverse Drug Reaction process

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2:01

Investigational New Drug (IND)

Cliniminds India

Shared 9 months ago

131 views

12:46

Regulatory writing / Medical Writing - CMC Module

Cliniminds India

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558 views

10:17

New drugs and clinical trial (NDCT) rules 2019

Cliniminds India

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19:17

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

Cliniminds India

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