White Papers Sitemap

Need of Good Laborarory Practices

INTRODUCTION

HISTORY OF GLP

NEED OF GLP

MANAGEMENT PROCESS OF GLP

CONCLUSION

NEED OF GOOD LABORATORY PRACTICES

GLP is needed to regulate all non-clinical safety studies that supports research and marketing permits for a product including veterinary drugs, aroma and color additives in food, medical devices and other bio-products. GLP can be applied to short term as well as long term studies. This regulation is a must for:

Non-clinical safety studies of drug development process.
Agricultural pesticide development
Development of toxic chemicals
Testing of substance for explosive hazards
Food Control

CORE SERVICES

Clinical Trial Material Logistics Management Services

Pharmaceutical Regulatory Affairs

IVRS Based Services in Clinical Research

Clinical Research Contract Management

IT Services in Clinical Research

E-Learning

WHITEPAPERS

Drug Development Process

Future of Clinical Research

Data Standards in Clinical Trials

Electronic Data Capturing: A Boon for Clinical Trials

Using IVRS for Clinical Trial Management.

Why Chose India for Conducting Clinical Trials ?

Importance of Regulatory Affairs in Clinical Research.

Good Manufacturing Practices.

Good Laboratory Practices.

An Insight into Good Clinical Practices.

Career Options in Clinical Research.

Clinical Research | Regulatory Affairs | IT Services | E-Learning
home | About us | Career | Collaboration | Why Us | News Room | Blogs | Contact Us

Contact Fermish

FERMISH CLINICAL TECHNOLOGIES PVT. LTD. - Tel : +91-11-30885160 - Mail : contact@fermish.com

D - 115, Okhla Industrial Area, Phase - I, New Delhi - 110020, India