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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3:09

Pharmacovigilance System Master File

Cliniminds India

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3:16

Cliniminds – Bioavailability & Bioequivalence Studies

Cliniminds India

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7:42

Qualified Person for Pharmacovigilance QPPV

Cliniminds India

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6:11

Qualified Person for Pharmacovigilance - QPPV

Cliniminds India

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3:43

SOPs and Procedural Documents - PHARMACOVIGILANCE AUDITS & INSPECTIONS

Cliniminds India

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4:33

PV Workflow - PHARMACOVIGILANCE AUDITS & INSPECTIONS

Cliniminds India

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8:10

Cliniminds Orientation : Drug Regulatory Affairs, IPR & Patents

Cliniminds India

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3:37

Cliniminds Dossier preparation and submissions: Drug Regulatory Affairs

Cliniminds India

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210 views

4:14

Career Opportunities in Drug Regulatory Affairs & IPR

Cliniminds India

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3:05

CLINIMINDS CASE REPORT FORMS - CLINICAL RESEARCH

Cliniminds India

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4:02

Protocol Design - Clinical Research

Cliniminds India

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4:03

CTD (Common Technical Document ) Module 1

Cliniminds India

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276 views

4:07

Cliniminds Literature search - Pharmacovigilance

Cliniminds India

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3:07

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

Cliniminds India

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215 views

18:46

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

Cliniminds India

Shared 4 months ago

252 views

1:03:36

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

Cliniminds India

Shared 5 months ago

335 views

4:42

International Council for Harmonisation (ICH)

Cliniminds India

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176 views

4:17

Pharmacovigilance Programme of India (PvPI)

Cliniminds India

Shared 6 months ago

643 views

3:56

Common Technical Documents - Drug Regulatory Affairs

Cliniminds India

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258 views

3:05

Naranjo Scale - Pharmacovigilance

Cliniminds India

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3:26

Data Management Plan (DMP) - Clinical Data Management

Cliniminds India

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3:00

Database Lock Point - Clinical Data Management

Cliniminds India

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2:46

Principal of ALCOA+ in Clinical Data Management

Cliniminds India

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1:02

When did the formal celebration of Clinical Trials Day begin?

Cliniminds India

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2:48

User Acceptant Testing - Clinical Data Management

Cliniminds India

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657 views

2:46

Clinical Trial Agreement (CTA) - Clinical Research

Cliniminds India

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147 views

3:37

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

Cliniminds India

Shared 7 months ago

255 views

5:30

Introduction of Aggregate Report

Cliniminds India

Shared 7 months ago

266 views

4:45

eCRF Completion Guidelines

Cliniminds India

Shared 7 months ago

227 views

0:29

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

Cliniminds India

Shared 7 months ago

164 views

2:52

Audits and inspection in Clinical Research

Cliniminds India

Shared 7 months ago

132 views

7:35

Why 'Results' Are the Heart of Medical Writing

Cliniminds India

Shared 7 months ago

126 views

2:55

Clinical Research| where clinical trials take place?

Cliniminds India

Shared 7 months ago

61 views

3:09

The Importance of Probing in Adverse Events

Cliniminds India

Shared 7 months ago

45 views

8:20

Medical Device Regulation - Regulatory Affairs

Cliniminds India

Shared 8 months ago

320 views

8:46

Orientation Session of Pharmaceutical Business Analytics - 23rd March 2025

Cliniminds India

Shared 8 months ago

119 views

8:40

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

Cliniminds India

Shared 8 months ago

250 views

6:56

eCTD Software Training – Drug Regulatory Affairs

Cliniminds India

Shared 9 months ago

2.4K views

5:48

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

Cliniminds India

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307 views

9:30

eTMF Software Training

Cliniminds India

Shared 9 months ago

518 views

7:32

Aggregate reports (PSUR)

Cliniminds India

Shared 9 months ago

293 views

4:51

Overview of Healthcare Systems in United States - Healthcare Analytics

Cliniminds India

Shared 9 months ago

580 views

7:43

Epidemiology - PHARMACEUTICAL BUSINESS ANALYTICS

Cliniminds India

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104 views

6:05

Importance & Composition of Ethics Committee

Cliniminds India

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273 views

19:58

Health Technology Assessment (HTA) in Europe - HEOR

Cliniminds India

Shared 10 months ago

216 views

6:52

Investigator and Site Selection - Monitoring of Clinical Trials

Cliniminds India

Shared 10 months ago

191 views

5:44

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

Cliniminds India

Shared 10 months ago

295 views

8:32

Responsibilities of Ethics Committee- PPT Presentation By Anjali Bachulkar

Cliniminds India

Shared 10 months ago

204 views

4:19

Clinical Trial Registries -PPT Presentation By Keerthi S

Cliniminds India

Shared 10 months ago

144 views

8:06

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

Cliniminds India

Shared 10 months ago

489 views

7:12

Phase 3 Clinical Trial PPT Presentation By Anvita Gangan

Cliniminds India

Shared 10 months ago

292 views

4:14

PADER Report (Periodic Adverse Drug Experience Report)

Cliniminds India

Shared 10 months ago

460 views

8:30

Computer System Validation (CSV)

Cliniminds India

Shared 10 months ago

1.1K views

5:59

The Republic Day celebration by Cliniminds Students and Teachers

Cliniminds India

Shared 10 months ago

65 views

6:57

Creation of Data Transfer documents - Clinical Data Management

Cliniminds India

Shared 10 months ago

320 views

21:18

Emerging Global Trends in Pharmaceutical Regulatory Affairs

Cliniminds India

Shared 11 months ago

216 views

5:27

Importance of External Data - Clinical Data Management

Cliniminds India

Shared 11 months ago

249 views

11:01

Regulatory framework in the European Union - Drug Regulatory Affairs

Cliniminds India

Shared 11 months ago

794 views

6:45

Drug Master File - Regulatory Affairs

Cliniminds India

Shared 11 months ago

223 views

9:09

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

Cliniminds India

Shared 11 months ago

207 views