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Industrial Pharmacy  5th Semester B.Pharmacy Assignments,BP502T Formulative (Industrial) Pharmacy,Handwritten Notes,Question and answers,BP502T Formulative (Industrial) Pharmacy,B. Pharmacy 7th Semester,

Industrial Pharmacy

B.Pharmacy, 5th Semester, 2024 (2023-2024) - Assignments

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60 2 Report May 08, 2024

Industrial Pharmacy B.Pharmacy 5th Semester 2024 (2023-2024) Previous Year's Question Papers/Notes Download - HK Technical PGIMS



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Industrial Pharmacy

Industrila Pharmacy

  1. What is master formula record?
  2. Write the principles of quality risk management.
  3. Enumerate the objective of TIFACs.
  4. Name different types of drug applications that can eb submitted to FDA.
  5. What are the objectives of ICH guidelines?
  6. what are the benefits of ISO 9000?
  7. List out the significance of NABL accredition.
  8. Define medical device and give 2 examples.
  9. Give 2 applications of biostatics in pharmaceutical product development.
  10. How equipments are categorised based on SUPAC guidelines?
  11. Differentiate qualification and calibration of equipment.
  12. Write the primary functions of APCTA.
  13. Write the purpose of confidential agreement.
  14. Mention the davantages of QbD.
  15. Define clinical trails and write its importance.
  16. Define biostatistics.
  17. What are the objective sof OOS?
  18. Name the TT agencies in India.
  19. What is platform technology?
  20. What are objectives of GLP?
  21. What is CTD?
  22. List out various regulatory authorities?
  23. Write the functions of TIFAC?
  24. Name 2 significance of NDA.
  25. Write the benefit of pilot plant scale up techniques.
  26. What are the elements of QbD?
  27. Classify changes and give examples.
  28. What are the significance of CTD?
  29. Name any 4 general requirements for pilot plant construction.
  30. What are the steps involved in technology transfer?
  31. Name the contents of batch manufacturing record.
  32. Write the features of TBSE?
  33. Define TDM and what are the key features of TDM?
  34. Enlist the benefits of ISO 14000.
  35. Salient features of ISO 9000.
  36. Primary objectives of NRDC.
  37. Write 2 reasone for TT in pharmaceutical industry.
  38. Define validation and qualification.
  39. Name types of studies involved in pre-clinical drug development.
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