Tablet dosage form defects solving the problem
Question: How to solve this problem of Capping in tablets, we are getting consistent problem of capping in our Paracetamol tablets where paracetamol is 500 mg and other excipients like…
Document Control System in a Pharmaceutical Company
Documentation control In a Pharmaceutical Manufacturing Company Standard operating procedure is the originator of the documents, in a standard operating procedure instructions are provided for doing an activity. In the…
Data Integrity how to maintain Data Integrity
Data Integrity is very important aspect of pharmaceutical good manufacturing practices. We have provided here a presentation for training personnel in Pharmaceutical manufacturing company.
Quality management system in Pharmaceutical Company
Quality management system in a pharmaceutical manufacturing company What is quality management system QMS in pharma company? Following functions all together when driven together forms, every function is more or…
Important aspects of Deviation how to handel
What you should know for effective handling deviations in a pharmaceutical company Definition of Deviation: Any observed and non-observed departure of value or an event or procedure or action from…
How to handle investigate and identify root cause of a market complaint of a drug product.
How to handle market complaint in pharmaceutical industry? One of the prime objective of addressing the market complaints or product complaint received from user is to 1) Prevent any loss…
Air handling Unit
Clean Room
Clean room Classification
Pharmaceutical Manufacturing
US FDA Guidelines
Clean room classification In Pharmaceutical Industry Guidelines
Clean Room Classification in pharmaceutical Industry how it is done?. What is a clean room in Pharmaceutical Manufacturing?. Which are the different requirements of clean room class in pharmaceutical manufacturing…
Revalidation in pharmaceutical manufacturing when why to do Revalidation
Revalidation in pharmaceutical manufacturing its regulatory and general requirements. Validation in pharmaceutical is not only mandatory by law or regulation, but also it a is one of the method by…
Pharmaceutical Area classification with respect to filters used as per WHO guidelines
Pharmaceutical Area classification with respect to filters used as per WHO guidelines WHO gmp guidelines describes area in a pharmaceutical Manufacturing facility, as Level 1 level 2 and level 3…