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B. Pharmn
Total No.^ of^ Pages:^1 BPHT
7 Semester^ Examination:^ December^2021
PHARMACY PRACTICE
Full Marks: 75 Time:3^ Hrs.
Answer (^) Part-A, Part-B^ &^ Part-Cas per the^ instructions^ there^ in. The (^) figure in^ the^ right hand^ margin^ indicates^ marks
PART-A
[10x2-20]
- Answer All a) Write different types of hospitals.
b) Define^ the^ term^ medical^ adherence.
c)What do^ you^ understand^ by^ medication^ history?
d)What do^ you^ mean^ by^ drug^ information^ bulletin?
Write (^) any two^ roles^ of^ pharmacist^ in^ the^ education^ and^ training^ program. What is (^) your understanding on^ over^ the^ counter^ drug? gWhat are^ the^ clinical^ significance^ of^ thrombocytes?
h) What^ is^ the^ significance^ of^ therapeutic^ drug^ monitoring?
1) What^ do^ you^ understand^ by^ medication^ error?
j) What^ is^ the^ fundamental^ objective^ of^ community pharmacy^
management?
PART-B
[2x10-20]
- Answer any T wo: a) Discuss^ in^ detail^ about^ adverse^ drug^ reaction and^ its^ reporting for^ proper interpretation. b) Give^ a^ detail^ events^ on^ patient^ counseling^ and add a^ note^ on^ patient counseling in hypertension. c) Give^ a^ salient^ features^ on^ organization^
of (^) drug store^ and^ add^ a^ note^ on purchasing and^ inventory^ control^ in^ an^ ideal^ drug^ store.
PART-C (Answer^ any^ Seven)^ 7x5-35]
- Write^ a^ short^ note^ on^ hospital^ pharmacy^ and^ its^ organization.
4. Enumerate^ briefly^ on^ Pharmacy^ and^ Therapeutic^ Committee.
What are^ the^ contents^ of^ hospital^ formulary?
- Write^ a^ short^ note^ on^ therapeutic^ drug^ monitoring.
- What^ are^ the^ functions^ and^ responsibilities^ of a clinical (^) pharnmacist? 8.9. (^) HowWhat a budget is prepared in the pharmacy department ofare^ the roles^ of^ hospital^ pharmacist^ in^ the^ investigational any hospital?^ drugs?
- Write^ short^ note^ on^ any^ Two^ of^ the^ following: a) Community pharmacy b) Drug^ distribution^ system^ ina^ hospital c) Abnormal^ constituent^ of^ urine
(2x2.5)
Total No.^ of^ Pages:^1 B.^ Pharm BPHT 7th Semester Examination: December 2021 INDUSTRIAL PHARMACY-I
Full Marks: 75 Time:^3 Hrs.
Answer Part-A, Part-B & Part-C as per the instructions there in.
The figure in^ the^ right^ hand^ margin^ indicates^ marks. PART-A [10x2-20]
- Answer All a. What is pilot plan scale up? b. Define APCTD and TIFAC?
C. Define OOS?
d. Define QbD and write the Objectives of QbD? What do you mean by Quality risk management? Discuss about Investigator's Brochure? g. Discuss about the ISO 9001 quality system? h. Define the term "Regulatory Affairs"?
e.
f.
i. Discuss^ about^ DMF?
j. Differentiate^ between^ BE^ and^ BA?
PART-B3 [2x10-20]
- Answer any Tw a)a) What is pilot plant scale up? Discuss the significance and requirements for scale up of pharmaceutical product from R and D to plant. b)b)^ Discuss^ general^ considerations^ of^ Investigational^ New^ Drug^ (IND)
Application. Explain the role of biostatistics in pharmaceutical product
development.
c) What do you mean by the term "Technology Transfer"? Discuss in detail
about WHO^ guidelines for^ technology transfer.
PART-B(Answer any Seven)) (^) 17x5-35]
3.3.^ Define^ TQM?^ Role^ of^ TQM^ in^ Pharmaceutical^ Industry? Define QbD? Discuss about the tools of QbD? Briefly discuss^ about^ management^ of^ clinical^ studies?
- Discuss^ about^ the^ SUPAC^ guidelines.
- Write about Clinical research Phase Study? Discuss about Technology Transfer Protocol?
- Define GLP. How it helps to maintain quality of the product?
- Write details about CMC.
- Write short notes on any Two of following a) MoUs b) Documentation c) Quality Control
[2x2.5]
Total No.^ of^ Pages:^
(^2) B. Pharm BPHT 7th Semester Examination: December 2021 NOVEL DRUG DELIVERY SYSTEM Full Marks: 75 Time:^3 Hrs. Answer Part-A, Part-B & Part-C as per the instructions there in. The (^) figure in^ the^ right hand^ margin indicates^ marks. [10x2- PART-A
- Answer All a) Differentiate^ between^ sustain^ release^ and controlled^ release.
b) Drugs^ with^ short^ elimination^
half life are^ suitable^ for developmentment^
of
controlled release^ dosage form.^ True^ or^ False,^ Justify.
c)c) What^ is^ mucoadhesion? d)d) Describe^ the^ role^ of osmotic^ agents in^ osmotic^ pump^ with^ examples.
e)e) Differentiate^
between matrix^ and^ reservoir^ system.
) Explain^ about^ the significance of^ absorption^
window of^ drug in
developmet of GRDDS.
- Differentiate^
between liposome and^ niosome.
h) What^ are^
the advantages of^ intrauterine^
devices?
Give some^ examples^ of^ hydrophilic^
and hydrophobic polymers
i)
j) What^ are^
the crieteria^ for^ selection^ of^ drug^
as trandermal^ DDS.
[2x10-20]
PART-B
- Answer^ any^ Two:- Describe in^ detail^ about various^ approaches^ used^ in^ the^ design^ of a) controlled formulations^ by^
diffusion and^ dissolution^ principles^ with^ neat
labeled diagrams. What is^ microencapsulation.^
Write the^ names^ of^ various^ methods^ of microencapsulation. Desribe^ in^ detail^ about^
coacervation phase separation
method of microencapsulation. What are the basic components of transdermal drug delivery systems. Describe the^ formulation^ approaches^ in^ the^ design^ of^ TDDS^ with diagrams.
b)
PART-C (Answer^ any^ Seven) [7x5-35]
- Write about the applications^ of^ polymers^ in^ controlled relase formulation development.
- Wirte about any two approaches in the development of gastro-retentive formulations.
- Discuss about the physicochemical properties of drugs relevant to controlled release formulation development.
- Write^ about^ the^ principles^ of^ bioadhesion/mucoadhesion.
Enumerate the intra ocular barriers and methods to
overcome ocular drug
delivery.
8. Write about ant two
methods of preparation of
9. What are the liposomes.
different methods of characterization of
10. Write short note on microcapsules
any Two^ of^ the^ following:
a) Metered dose inhalers
b) Monoclonal antibodies
c) Osmotic pump
(2x2.5)
