Found 58 presentations matching your search
Phase-by-Phase Clinical Trial Costs explained with detailed insights on budgeting, patient expenses,...
Contract Research Organisations- An Overview in Pharma Field
describe about role of sponsor and CRO on clinical trial process
contract research organization
Basics of Clinical Research
Establishing pharmacovigilance programme
Introduction to CONTRACT RESEARCH ORGANIZATION, Background, Over all view of CRO Presented by G.Ar...
When a new drug/device/surgical procedure/treatment or other potential medical innovation is develop...
clinical research
As of my last knowledge update in September 2021, the list of the top Contract Research Organization...
Working on Clinical Trials – Getting started Very few clinical trials are conducted only in one c...
This presentation comprises information about clinical trial supply management.
the slide is about basic concept of the clinical trials
schedule y
A brief introduction of clinical sas programming
Essential documents for conduct a clinical trials
A standard for the design, conduct, performance, monitoring, auditing, recording, analyses and repor...
This presentation is a brief overview of ICH-GCP guidelines. Although ICH-GCP is a very vast topic, ...
Regulatory writing
Clinical Trials
Roles and Responsibilities in Clinical Trials of Investigator, Study Coordinator, Sponsor, Monitor, ...
Preparation of protocol M.pharm SEM II pharmacovigilance
Phase 0 and Phase 1 Clinical Trial
![Indian gcp guidelines[647]](https://slidepub.com/thumb/6561/245026561.jpg)
