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MedDRA is a terminology used in pharmacovigilance which is used in coding the different aspects in c...
Evaluating the Efficacy of Shatavari Churna in Pittavrita Vyana Vayu: A Single-Arm Clinical Study w....
Contents Guidelines for Preparation of Documentation Clinical Study Reports Clinical Trial Monitorin...
Clinical study reporting is a critical and complex process in the development of new medical treatme...
Regulatory reporting is a fundamental aspect of scientific research and is crucial for ensuring comp...
What are Good Documentation Practices? In the context of these guidelines, good documentation practi...
A document outlining trial objectives, design, methodology, and analysis plan.��It serves as a r...
Clinical Data Management (CDM) is a critical component of clinical research that involves the collec...
Study designs are fundamental frameworks that guide the planning, execution, and interpretation of r...
Good Clinical Practice (GCP) guidelines are a set of international ethical and scientific standards ...
Definition of Materia Medica (MM): Materia Medica in Homoeopathy refers to a systematic compilation ...
Pubrica’s team of researchers and writers create scientific and medical research articles, which m...
An Individual Case Safety Report (ICSR) is a report of an adverse event or suspected adverse reactio...
Turacoz Skill Development Program tells you about the medico-marketing, its objectives, ethics foll...
Site n-Alysis™ allows you to identify and qualify potential study sites based on surrounding patie...
Turacoz Skill Development Program provides medical writing training on various types of regulatory d...
SAE data reconciliation The process of comparing key safety data variables between the drug or devic...
It gives information about CTD and eCTD. Also, please learn about their similarities and differences...
Forty-six million people worldwide are living with bipolar disorder, typically treated with medicati...
Created by: Mr. Attuluri Vamsi Kumar, Assistant Professor, Department of MLT, UIAHS, Chandigarh Univ...
COMMON TECHNICAL DOCUMENT AND ELCTRONIC COMMON TCHNICAL DOCUMENT
- Whilst the realization of the CTD took many years, there is now a common format for the submission...
The Common Technical Document (CTD) is a standardized format for regulatory submission of informatio...
LIST OF ALL THE ESSENTIAL DOCUMENTS REQUIRED IN A CLINICAL TRIAL
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