Tuesday, November 24, 2020

Lighting in Pharmaceutical Areas

Light intensity plays important role for better work at work place. Light intensity levels effect on the systolic and diastolic blood pressure, blood oxygen...

Passivation of Stainless Steel in Pharmaceuticals

Passivation Basics: The term Passivation originates from the word "Passive". Passivation is a natural phenomenon in which an inert layer is formed on the surface...

Cleanrooms for Aseptic Processing

Cleanrooms are used in practically every industry where small particles can adversely affect the manufacturing process. They vary in size and complexity, and are...

WHO: Draft on GMP for HVAC-Systems for Non-Sterile Pharmaceuticals

During a consultation on data management, bioequivalence, GMP and medicines inspection held by the WHO in 2015, a revision of the Supplementary Guidelines on Good...

Different Storage Conditions in Pharmaceuticals

According to the pharmaceutical drug material different storage conditions are required to maintain their quality. Some chemicals and solutions in quality control and media...

USP/NF Storage Temperature

Storage temperature is very important in maintaining the efficacy, potency and stability of drugs. Because drugs are temperature dependent and a factor which cause them to deteriorate and...

Data is Omnipresent now a days so Data Integrity is a key concern

Data a longest lasting commodity for any company. Auditors favourite destination. If controlled best adds to Quality and Reputation of the firm. It needs to...

Data Integrity: 5 Question Need to ask !

For several years now, data-integrity violations have been the main reason why the US Food and Drug Administration (FDA) has issued warning letters to...

Difference between Deviation and Incident in Pharmaceutical

Differentiation between Deviation and Incident in pharmaceutical GMP manufacturing facility. Deviation is departure from the written procedure, incident there is no procedure, it is basic understand,...