B Pharm 7th Industrial Pharmacy 2 Imp Questions 2024

In this post b pharm 7th Industrial Pharmacy 2 important questions are given for 2024. 

Many of these questions are likely to be asked in the exam. 

In preparing this question set and making the exam useful, the help of previous question papers and industrial pharmacy 2 question bank has been taken. 

Some of the questions given here are very important because those questions are being asked many times and continuously. 

Therefore, take this set seriously and prepare its answers. 

The most important thing is that you have to prepare the answers by writing in your own words. 

For this, your concept should be clear on the Industrial Pharmacy topic. 

How will this happen? 

A simple solution for this is to read the topic related to B pharm 7th sem ip 2 imp questions given here in your textbook 2 to 3 times and understand its meaning. 

Once you understand the lesson's meaning, you can easily write answers to these and many more questions. 

By solving the set of questions given here, you can prepare excellent and exam-useful notes on the Industrial Pharmacy topic for yourself. 

To solve the questions of industrial pharmacy ii question paper based on this topic, you can also take the help of your university professor and advanced book. 

You can also use this question set as a practice paper. 

You will find more such sets available on the internet for practice. 

Which can be downloaded and used.

After solving this set your confidence level will definitely increase. 

To select the questions given here, the help of IP 2 previous year question papers and question papers of many other universities have been taken. 

From this Industrial Model Paper, you will get accurate information about the patterns of questions and the format of question papers in the examination hall. 

When you get the question paper of industrial pharmacy 7th sem question papers for bpharm in the examination hall, then first check the entire question paper page by page. 

In case of any error, request a fresh question paper from the invigilator. 

Try to write an accurate and informative answer using as many words as are recommended in the instructions on the first page of the question paper. 

This will save you time and you will be able to devote time to other questions also. 

After writing all the questions, revise your written answers once in the examination hall itself. 

Confirm whether you have written the answers to all the questions or not. 

Let's solve these industrial pharmacy 7th sem important questions.


Industrial Pharmacy 2 Questions

Important Questions For B Pharm Industrial Pharmacy 2 7th Semester

  • Write about GMP considerations in pilot plant scale-up.
  • Enumerate the agencies for Technology Transfer in India. Write the Technology Transfer-related documentation.
  • Define clinical trial according to CDSCO.
  • Define Certificate Of Pharmaceutical Products (COPP). Discuss the purpose, scope, importance, types, and functions.
  • What are the three aspects of TQM?
  • Define Investigational New Drug (IND). Classify them, mention their types of application, and layout chart for IND application.
  • Discuss the pilot plant scale-up considerations for solids.
  • Define Pilot plant scale. Write a short note on pilot plant scale-up consideration for liquid orals.
  • Write short notes on the following:- (a) Phases for clinical trials (b) USFDA.
  • What are the responsibilities of State Licensing Authorities?
  • Write short notes on the following:- (a) SUPAC (b) Investigator’s Brochure (c) Drug Testing Laboratories.
  • What are the components of non-clinical drug development?
  • Write a note on Analytical Method Transfer.
  • State about slugging.
  • Explain the Bioequivalence studies.
  • Explain the Organization and responsibilities of the Central Drug Standard Control Organization.
  • Write a short answer on Six Sigma concepts.
  • Write the Application of biostatistics in pharmaceutical product development.
  • What is the scope of pharmaceutical QMS?
  • Write a short note on the approved regulatory bodies & agencies.
  • Write the organizational structure of CDSCO.
  • What is meant by NABL certification?
  • Write a short answer on the following:- (a) CDSCO (b) QbD (c) WHO (d) ISO 9000 (e) Change Control.
  • Write the concepts of quality.
  • Expand the term "BCIL and NRDC".
  • Explain the Quality Risk Management.
  • Explain the Standard Operating Procedure.
  • What is a Clinical Trial?
  • Write a short note on the following:- (a) Drug Master File (DMF) (b) New Drug Application.
  • Explain the term 'ANDA'.
  • What is NABL?
  • Write short answers on the following:- (a) Drug Development Teams (b) Non-clinical drug development (c) Note on GLP (d) Central license approving authority.
  • Write a short notes on ISO 14000.
  • Describe in detail the role and responsibility of the regulatory affairs department.
  • Define In-process control. 
  • Discuss the principles, advantages, needs, and scope of NABL.
  • What are Good Laboratory Practices?
  • What is total quality Management?
  • What is the purpose of pre-clinical testing?
  • Write a short answer on the requirements for permission of NDA.
  • What are BE & BA studies?
  • Where clinical studies are conducted?
  • Write a short note on post-marketing surveillance.
  • What is 'DTAB'.

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