Lark Laboratories (I)
Jaypee Healthcare Interview Questions and Answers
Q1. How many pressure is release opening a door of any section.
The question is not clear and requires more information.
The question needs clarification on which type of door and section is being referred to.
The pressure required to open a door can vary depending on the size and weight of the door.
It is important to consider the safety regulations and standards for pressure release in a production facility.
Without more information, it is difficult to provide a specific answer to this question.
Q2. What is difference between syrup and elixir?
Syrup is a concentrated solution of sugar in water, while elixir is a sweetened, flavored, and medicated liquid.
Syrup is used as a sweetener and flavoring agent in food and beverages.
Elixir is a medicinal preparation that contains active ingredients.
Syrups are usually thicker and more viscous than elixirs.
Elixirs are often used to mask the unpleasant taste of medicines.
Examples of syrups include maple syrup and corn syrup, while examples of elixirs include cough syrup and pai...read more
Q3. How to range (light)of tablet inspection.?
The range of tablet inspection can be determined by considering factors such as size, shape, color, and texture.
Consider the size of the tablets being inspected
Take into account the shape of the tablets
Consider the color and texture of the tablets
Use appropriate lighting and magnification to aid inspection
Ensure that the inspection process is consistent and standardized
Q4. What is the tablem and types of tablet .
Tablets are solid dosage forms containing active pharmaceutical ingredients and excipients compressed into various shapes and sizes.
Tablets can be classified based on their method of preparation, such as compressed tablets, molded tablets, and coated tablets.
They can also be classified based on their release mechanism, such as immediate-release, extended-release, and delayed-release tablets.
Examples of tablets include aspirin tablets, paracetamol tablets, and multivitamin tab...read more
Q5. What is GMP
GMP stands for Good Manufacturing Practice. It is a set of guidelines that ensure the quality and safety of pharmaceutical products.
GMP is a system of quality control that covers all aspects of pharmaceutical production.
It includes guidelines for the design and construction of facilities, equipment, and processes.
GMP also covers the training and qualifications of personnel, as well as documentation and record-keeping.
Examples of GMP requirements include proper sanitation, val...read more
Q6. What is cgmp
CGMP stands for Current Good Manufacturing Practice. It is a set of regulations enforced by the FDA to ensure quality and safety in pharmaceutical manufacturing.
CGMP is a set of guidelines that ensure the quality and safety of pharmaceutical products.
It covers all aspects of the manufacturing process, from raw materials to finished products.
CGMP requires manufacturers to maintain detailed records and follow strict procedures to prevent contamination and ensure consistency.
Exa...read more
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