Quality control is a department where the drug quality is tested, checked and confirms a drug fulfills the regulatory requirement with respect to safety, quality and efficacy.
In the pharmaceutical industry, stability chambers are designed to store the drug product or material in different storage conditions. Let’s understand What are stability chambers …
Difference between OOS-OOT-OOC-OOE: When it comes to handling deviations in analysis results, the terms OOS, OOT, OOC and OOE always come up. But how are …
Types of pH meter in pharma: Ph meter is one of the instrument used in the pharmaceutical industry to measure the pH of the water …
Principle, Types And Application Of Acid-Base Titration: In laboratories, titration is used to determine the concentration of a specific analyte through quantitative chemical analysis. It …
Pharmaceutical companies tout the safety of their new drugs. However, when FDA inspectors visit the production facility, the work is immediately halted; vital quality control …
Preparation and standardization of potassium Hydroxide: Here we will understand how to do preparation and standardization of potassium hydroxide (KOH) as per USP. Reagents required: …
UPLC Advantages Over HPLC: Even though the working principle of UPLC and HPLC are the same but UPLC is a more advanced separation technique as …
UPLC Principle: It is a technique used to separate any sample into its constituent parts via liquid chromatography. There is no real fundamental difference in …
4 Different Types Of Titration In Pharma: Different types of titrations can be classified according to the substance being evaluated or the type of analysis …
IR Do’s And Don’ts In Pharmaceuticals: Do’s of IR: Whenever any error massage is displayed on the monitors, immediately inform to instrumentation engineer. Example: error …