Akums Drugs & Pharmaceuticals Limited
Y-Axis Overseas Careers Interview Questions and Answers
Q1. What's S1, S2 and S3 in dissolution?
S1, S2, and S3 in dissolution refer to the stages of dissolution testing in pharmaceutical analysis.
S1 is the stage where the tablet starts to disintegrate into smaller particles.
S2 is the stage where the drug starts to dissolve into the surrounding medium.
S3 is the stage where the drug is completely dissolved and available for absorption.
These stages are important in determining the release rate of the drug from the dosage form.
Q2. What's Q stands for in Dissolution?
Q stands for Quantity in Dissolution.
Q stands for Quantity in Dissolution testing.
It refers to the amount of drug substance that is dissolved in a specified time period.
It is an important parameter in assessing the quality and performance of a drug product.
Q can also stand for Quality in some contexts, but in Dissolution it specifically refers to Quantity.
Q3. What's Normality, Molarity and Molality?
Normality, Molarity, and Molality are different units of concentration used in chemistry.
Normality is the number of equivalents of a substance dissolved in a liter of solution.
Molarity is the number of moles of solute per liter of solution.
Molality is the number of moles of solute per kilogram of solvent.
Normality is used in acid-base reactions, while Molarity and Molality are more commonly used in general chemistry.
Example: A 1M solution of NaCl has 1 mole of NaCl dissolved ...read more
Q4. What is UV and Visible Range?
UV and visible range refer to the wavelengths of electromagnetic radiation that are visible to the human eye.
UV range typically refers to wavelengths between 10-400 nm, while visible range refers to wavelengths between 400-700 nm.
UV radiation is divided into UVA (315-400 nm), UVB (280-315 nm), and UVC (100-280 nm).
Visible light is the portion of the electromagnetic spectrum that is visible to the human eye and includes colors from violet to red.
UV and visible range are common...read more
Q5. What's principal of HPLC
HPLC stands for High Performance Liquid Chromatography, a technique used to separate, identify, and quantify components in a mixture.
HPLC involves a stationary phase, a mobile phase, and a detector.
The sample is injected into the system and carried by the mobile phase through the stationary phase.
Different components in the sample interact differently with the stationary phase, leading to separation.
The detector measures the amount of each component as it elutes from the colu...read more
Q6. What's Dissolution stages
Dissolution stages refer to the different phases in which a solid substance dissolves in a liquid medium.
Dissolution begins with the solid substance breaking down into smaller particles
The smaller particles then disperse in the liquid medium
Finally, the particles fully dissolve and become uniformly distributed in the liquid
Q7. What's ALCOA+++?
ALCOA+++ is a set of principles for data integrity in the pharmaceutical industry.
Attributable
Legible
Contemporaneous
Original
Accurate
Complete
Consistent
Enduring
Available
Traceable
Q8. What's OOS and OOT?
OOS stands for Out of Specification and OOT stands for Out of Trend.
OOS refers to a result that falls outside the acceptance criteria specified in the test procedure.
OOT refers to a result that shows a trend outside the expected range over time.
Both OOS and OOT results may indicate potential issues with the quality or consistency of the product being tested.
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