PharmaWhiz

01/11/2020

“Better the Management Review, Better the performance of organization will be.”
How to do management review effectively - Read More
http://blogs.pharmawhiz.com/management-review-in-pharmaceutical-industry/

27/08/2020

http://blogs.pharmawhiz.com/risk-management-approach/

28/06/2020

You will see new feature on Pharmawhiz very soon

24/05/2020

Trend Analysis - tool for risk-based thinking
http://blogs.pharmawhiz.com/trend-analysis-tools-for-risk-based-thinking/

04/04/2020

https://www.pulse.qa/poll/doing-trend-analysis-qms-apply-risk-based-thinking

Are you doing Trend analysis in QMS to apply Risk-Based Thinking…

11/03/2020

COVID-19 (Corona Virus) and Unethical Business
On one side, China & other countries across the world are struggling with the infection of COVID-19 (Corona Virus) and on the other side, some selfish people are selling unapproved products in the market and they are claiming that these products are effective to fight with COVID-19

14/02/2020

As stated by Orange Guide 2002, human error is responsible for the majority of defective medicinal products that impact the patient’s health badly so keeping this in view, it is necessary to identify and control the possibility of human error in the pharmaceutical environment.

http://blogs.pharmawhiz.com/5-ways-to-reduce-human-error/

09/01/2020

In totality MHRA Inspectorate audited 286 facilities across the globe in the year 2018 and made total 6209 deficiencies EU GMP clause-wise all together as per its published deficiency report – 2018

A complete pharmaceutical & healthcare solution i.e. sharing knowledge with latest trend of articles, provide documents which have been prepared with consideration of current regulatory expectation as well as best industrial practicle knowledge and providing Raw material supplier information.

29/11/2019

A FDA warning letter on Quality Oversight and its analysis.

A complete pharmaceutical & healthcare solution i.e. sharing knowledge with latest trend of articles, provide documents which have been prepared with consideration of current regulatory expectation as well as best industrial practicle knowledge and providing Raw material supplier information.

10/10/2019

http://blogs.pharmawhiz.com/?p=311

How to prepare User Requirement Specification PharmaWhiz Author December 9, 2018 How to prepare User Requirement Specification2018-12-11T06:11:51+00:00 Equipment Qualification & Validation No Comment URS mean User Requirement Specification is a first document to define the procedure for the procurem...