Search Results for "regulatory authorities"

RutujaNale1

Pharmaceutical regulatory authorities and agencies

Organizational structure and application forms

39 slides 11,886

Regulatory affairs Historical overview of Regulatory Affairs, Regulatory authorities, Role of Regulatory affairs department

Historical overview of Regulatory Affairs, Regulatory authorities, Role of Regulatory affairs depart...

25 slides 911

Technology

role of regulatory authorities in detecting corporate frauds.pptx

corporate frauds

9 slides 38

PunitAgrawal17

Spontaneous ADR reporting system and reporting to regulatory authorities

Introduction Spontaneous ADR reporting process ADR reporting system in different countries Susp...

23 slides 1,507

yadavajay7077

The role and remit of regulatory authorities and FDA

Role and remit of regulatory authority and Food and Drug Administration

19 slides 1,162

ThasleemaParveenMoha

UNIT 2 Regulatory approval process and Regulatory authority and agency.pdf

Unit 2 Regulatory Approval Process Approval processes and timelines involved in Investigational New...

44 slides 14,954

Common Technical Document (CTD)

The Common Technical Document (CTD) is a standardized format for regulatory submission of informatio...

14 slides 993

An introduction to standard institutions and regulatory authorities such as ICH, WHO, USFDA, MHRA, TGA, BIS, ASTM, ISO, CDSCO

An Introduction to Standard Institutions and Regulatory Authorities such as ICH, WHO, USFDA, MHRA,...

30 slides 128

HemantAlhat1

ICH Guideline For Herbal Drugs.pptx

It is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss...

14 slides 32,910

Design

Good laboratory practices

GLP applies to nonclinical studies conducted for the assessment of the safety or efficacy of chemica...

41 slides 101,787

What is EPR Certificate?

EPR Certificate: An EPR (Extended Producer Responsibility) certificate is an official acknowledgmen...

8 slides 80

agileregulatory2

Protocol Writing in Clinical Research

Protocol writing is a critical phase in the planning and execution of clinical research studies. A w...

11 slides 385

Science

Turacoz - Clinical Study Report

“CSR is a detailed regulatory document which gives the information about the methods and results (...

39 slides 18,429

Ich – guidelines

ICH Guidelines were created by The International Council for Harmonization of Technical Requirements...

0 slides 631

Design

SKJAFARFAROOQUE

chapter4-220821134528-40197f10 Chapter 4 AAOIFI Standards.ppt

Chapter 4 AAOIFI Standards AAOIFI is responsible for developing and issuing standards for interna...

18 slides 32

Finance

AnfasChelembra

Financial Markets

Financial Markets - Money market-Organized and Unorganized-Sub markets Capital market- Primary marke...

140 slides 23,384

Finance

Companies Act, 2013

Companies Act - Companies Act, 1956 - Features - Types of Companies Act under the Act - Introduction...

24 slides 18,166

Maharashtra Public Trust Act, 1950.--pdf

The PPT Slides provide a comprehensive overview, guiding you through the Act's objectives, appl...

93 slides 1,098

Design

How 409A Value Services Reduce Litigation and Regulatory Risk?

409A valuation services reduce litigation and regulatory risk by ensuring stock options are priced a...

3 slides 1

409avaluations

Precision medicine.ppt

Precision medicine is an emerging strategy that considers individual variability in genes, environme...

21 slides 2,686

daltonmarketing

Developing and implementing effective RMPs to monitor drug safety post-approval.

Risk Management Plans (RMPs) are essential tools used by pharmaceutical companies and regulatory aut...

12 slides 28

ClinosolIndia

Regulatory Affair (Introduction) _Afzal Bano.pptx

*RA or government affairs, is a profession involved in monitoring and regulating the development, m...

10 slides 22

AfzalBano1

Clinical Trial Protocol

A clinical trial protocol is a comprehensive document that outlines the objectives, design, methodol...

23 slides 11,866