Self-Development & Thought Leadership

The World Economic Forum’s Global InformationTechnology Report 2016, explores some of the ways in which network readiness is essential to enabling the creation and use of emerging technologies.

The book has 43 chapters covering a range of issues organizations are fraught with in the current dynamic environment.Almost all of these are real, live cases describing situations middle to senior executives have dealt with, with a given amount of success.

The World Economic Forum’s Global InformationTechnology Report 2016, explores some of the ways in which network readiness is essential to enabling the creation and use of emerging technologies.

The book is a miniscule effort in the direction, its a mirror for our corporates to see what’s happening in this and an important part of the globe.

This book is neither a prescription nor an endorsement of any particular methodology discussed in the chapters but just the narration of the journey a few individuals in organizations have undertaken to better tackle the challenges they were facing.

In an unconventional and intriguing manner the author addresses the economics of quality, statistical thinking, statistical process control, and inspection efficiency. He provides a useful process model for achieving a continuous improvement state in any organization.

As the author is quick to say, “This is not a cookbook! It is, however, a book about cooking.”

Although similar to these recognized QMS standards, ISO/IEC 17025 serves a unique purpose: laboratory accreditation. It is not unusual for laboratories to retain dual certification to ISO 9001 and ISO/IEC 17025.

This handbook covers compliance with good manufacturing practices (GMPs), as regulated and guided by national and international agencies for the pharmaceutical industry. It covers finished human and veterinary drugs and biologics, and combination devices, as well as their component raw materials (including active pharmaceutical ingredients (APIs) and excipients), and packaging and labeling operations.

Although this handbook thoroughly prepares individuals for the ASQ CMQ/OE exam, the real value resides in post-exam usage as a day-to-day reference source for assessing quality applications and methodologies in daily processes. The content is written from the perspective of practitioners, and its relevance extends beyond traditional product quality applications.

This handbook covers compliance with good manufacturing practices (GMPs), as regulated and guided by national and international agencies for the pharmaceutical industry. It covers finished human and veterinary drugs and biologics, and combination devices, as well as their component raw materials (including active pharmaceutical ingredients (APIs) and excipients), and packaging and labeling operations.