• 1-800-526-8630U.S. (TOLL FREE)
  • 1-917-300-0470EAST COAST U.S.
  • +353-1-416-8900REST OF WORLD
Pharmaceutical Regulatory Inspections - Product Image

Pharmaceutical Regulatory Inspections

  • ID: 2776210
  • March 2014
  • Region: Global
  • 600 Pages
  • Euromed Communications

A unique and comprehensive guide to ensure regulatory compliance and success in pharmaceutical regulatory inspections.

In over 600 pages and twelve chapters this unique book provides a focused account of regulatory issues from pre-approval inspections and the inspection itself to postinspection and maintaining compliance. This is a book that every pharmaceutical company will wish to study before and during any inspection process to ensure a successful outcome.

Complete Remit

The book is a fully detailed and practical guide containing advice and insight to help any pharmaceutical organisation prepare for GMP Inspections, understand key regulatory issues and review inspectorate trends and findings.

Expert advice

The authors, with a wealth of regulatory experience behind them, express their views and provide useful and practical tips for succeeding in vital regulatory inspections.

International

The book includes chapters covering FDA Inspections, EU Inspections, Japanese Inspection and International Inspection processes.

Note: Product cover images may vary from those shown

1 Basic Concepts of Global GMP Requirements
by Tim Sandle and Madhu Raju Saghee

2 FDA Drug Regulation and Enforcement
by Seth Mailhot

3 System Based Approach to Inspections
by David Barr and Tim Sandle

4 Preparing for Preapproval Inspections
by Ron Johnson

5 Effectively Managing and Surviving FDA Inspections
by John Avellanet

6 Guide for Successful EU Inspection Management
by Siegfried Schmitt and Nabila Nazir

7 Regulatory Requirements of Japanese GMP Inspections
by Yoshikazu Hayashi

8 Preparing and Management of International Inspections
by Andreas Brutsche and Tim Sandle

9 Handling and Responding to Post Inspectional Observations
by Tim Sandle, Madhu Raju Saghee and David Barr

10 Preparing for Regulatory Inspections of Sterile Facilities: The Focal Points
by Tim Sandle

11 Preparing for Regulatory Inspections of API Facilities: The Focal Points
by Siegfried Schmitt and Richard Einig

12 Optimizing your Regulatory Compliance
by Mark Tucker

Note: Product cover images may vary from those shown

Edited by Madhu Raju Saghee
Quality Assurance, Micro Labs, and Director of PHSS, India

Foreword by Peter D. Smith
Vice President, Strategic Compliance, PAREXEL Consulting, USA

Note: Product cover images may vary from those shown
Note: Product cover images may vary from those shown

RELATED PRODUCTS

Our Clients

Our clients' logos