Trending of change controls shall be performed on quarterly basis and here i have given one example and Template to explain you about the Trending of change control. In order to prepare chart you have to use Excel sheet and according to your requirement you can use different types of charts. The below mentioned departments … Continue reading Trending of Change Control →

Human errors plays a major role in the violation of GMP and can lead to the deviation in different stages of manufacturing. Human errors have major or critical impact on products and may lead to the Data Integrity however due to various reasons human errors can occur which we have discussed in the earlier Topic. … Continue reading 9 ways to Reduce Human Errors in Pharmaceuticals and other industries →

In the below table i have mentioned some data integrity Risk Assessment Template for your reference and we can make such type of Assessment in other areas or systems or procedure also do pl go through this.

Hi dear Friends welcome to everyone to my blog including my daily readers and i have prepared one page which contains some factors which can lead to Human Errors ( but not limited to) How Mistakes Can Actually Make Employees Better When employees make a mistake at work (as we all do), they need to: … Continue reading Contributing factors that can lead to Human Errors in Pharmaceutical and other Industries →

Hi to All of My Readers and followers . I have prepared this interview questions based on my Experience which will be helpful to the senior position people. I have received so many request to post interview questions for senior position so today i am posting the same so pl read, understand and share if … Continue reading Top 30 Pharmaceutical Quality Assurance Interview Questions for Senior Positions →

Hi All This is Chandrasekhar panda having 14 years of Experience in Pharmaceutical Industry in Quality Assurance Department and above mentioned documents and other documents are available with me with latest MHRA & FDA Compliance and if any interested to purchase can contact me on jpanda1983@gmail.com and i can be reach in my whats app … Continue reading All Department SOPs, Change Control, Deviation, CAPA, Stability, Nitrosamine Impurity & Elemental impurity Risk Assessment, Quality Risk Assessment Case study, Process Validation Protocol & Reports →