04:42

How to get Certified in Clinical Trial Programming using SAS

02:46

Echocardiography

02:40

CTA - Computed Tomography Angiography

02:11

CT - Computed Tomography

03:17

Base SAS Certification

01:57

PACS - Picture Archiving and Communication System

02:16

MRI - Magnetic Resonance Imaging

02:06

DICOM - Digital Imaging and Communication in Medicine

01:52

DEXA - Dual Energy X-Ray Absorptiometry

02:25

Adverse Drug Reaction

02:24

How SAS is used to Analyze the Clinical Data

03:21

Clinical Research, Clinical Data Management and SAS

03:16

Modules covered in Clinical SAS

02:18

Post Marketing Surveillance (PMS)

01:56

IRB-Institutional Review Board

03:32

Medra Part II

02:38

Role of CRO's in Clinical Research

02:15

Basic Principals for Designing Clinical Trials

02:46

Protocol Indian GCP

02:20

Parallel Designs

02:50

Cross over designs

03:52

Data Handling and Record Keeping

02:31

Benefits of SOP in clinical trials

02:42

How SAS Works in Real Time Projects

02:21

Steps in SOP preparation for Clinical Trials

04:12

Protocl of a Clinical Research

03:11

Responsibilities of investigator

02:28

Purpose of Clinical trial

02:49

Phase I

02:57

Basics of phase III clinical trial

03:15

Serious Adverse Event

02:37

Non-compliance in clinical trials audit

02:00

Audit in Clinical Trials

02:44

Clinical Data Management and Statistical Analysis Software

02:22

Role of Biostatistician in Clinical Trials

02:56

Biostatisticians in Clinical Trials

03:03

Responsibilities of monitor indian GCP

02:41

Data Discrepancy

02:40

DRUG Master File

02:40

Different Case Report Form Modules

02:54

MedDRA

02:24

Premature Termination of Clinical Trial

02:06

Project Management in Clinical Trials

02:52

Serious Adverse Event

03:27

CRA in Clinical Trials

02:29

ICH Guidelines

01:39

Pre-Clinical Studies

01:04

Phase IV Clinical Trials

01:39

Data Handling and Record Keeping in Clinical Research

01:08

Case Report Form in Clinical Research

01:36

Responsibilities of Investigator in Clinical Research

01:44

CRC in Clinical Research

01:29

Informed Consent

01:14

phase 1 clinical trial

01:14

Responsibilities of Monitor in a Clinical Trial

02:15

ICMR general principles

01:26

How Traditional and Current SAS programmer Should be

01:21

Indian GCP.mp4

01:16

Pharmacovigilance in India.mp4

04:08

Certifications in SAS programming.