Tuesday, April 16, 2024

Three Different Types of Airlocks in Pharmaceuticals

Three Different Types of Airlocks in Pharmaceuticals Airlock helps to protect classified area that may occur during the men and material movement. “Air lock system” in...

Handling of Pharmaceutical Market Complaints (Regulatory requirements)

Complaint is defined as statement that is something wrong or not good enough, which shows customers dissatisfaction about the company or product. Market complaints are...

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...

Hold time study in Pharmaceutical Manufacturing

Hold time study in Pharmaceutical Manufacturing During pharmaceutical manufacturing sometimes in-process materials need to be hold more than usual. Hold time Hold time is a time period...

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...

Mixing Time Importance for Blend Uniformity

Mixing time during blending is an important factor. Extended mixing time can affected blend uniformity and pharmaceutical product quality. In pharmaceutical tablet manufacturing process more...

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...

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...

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...