Placeholder text

Deviation Management

Deviation Management

0 - Default Title
Description
Deviation handling plays a key role in assuring quality in Pharmaceutical products and by contributing to continuous improvement. Various Guidelines like WHO, ICH, EC GMP, SCHEDULE M mentions that deviation management is the regulatory requirement and be systematically handled for maintaining quality of pharmaceutical products .It is the important process of Quality Management System. Deviation is handled through a systematic process and a step wise explanation regarding procedure for Handling of Deviation is given as flow chart in the book. Important documents related to deviation like SOP, Deviation report, Log book are given in form of formats. To correct the deviation, finding the root cause is of prime importance and for that detailed Root Cause Analysis Process is explained. Change Control is an important process which handles changes as part of correction. Implementation of Corrective Action and Preventive Action(CAPA) is the outcome of deviation and plays a pivotal roll in correcting and avoiding future deviations. Book covers both change control process as well as CAPA in detail with necessary documents. Book also covers case studies for easy understanding of process.
Product details
Binding:
Paperback
Number of Pages:
96
Release Date:
2025-11-03
Publication Date:
2025-11-03
Publisher:
LAP LAMBERT Academic Publishing
Languages:
Original: English
ISBN10:
6209183980
ISBN13:
9786209183980
GPSR Manufacturer Reference:
Weight:
161 g
Height:
150 cm
Width:
220 cm
Thickness:
6 cm
Currently sold out