Exam Details
Subject | pharmaceutical technology-ii | |
Paper | ||
Exam / Course | b.pharm | |
Department | ||
Organization | Gujarat Technological University | |
Position | ||
Exam Date | May, 2017 | |
City, State | gujarat, ahmedabad |
Question Paper
Seat No.: Enrolment No.
GUJARAT TECHNOLOGICAL UNIVERSITY
B. Pharm SEMESTER-VIII EXAMINATION SUMMER 2017
Subject Code: 280002 Date: 29/04/2017
Subject Name: Pharmaceutical Technology-II
Time: 10:30 AM to 01:30 PM Total Marks: 80
Instructions:
1. Attempt any five questions.
2. Make suitable assumptions wherever necessary.
3. Figures to the right indicate full marks.
Q.1
Write note on in-process quality control test of tablet Mfg
06
Explain GMP with special ref. to personnel.
05
Give the difference between wet granulation and dry granulation
05
Q.2
Discuss the processing problems of tablets with remedies
06
Write a note on excipients and additives used in the capsule formulation
05
Classify cosmetics and write a short note on vanishing cream
05
Q.3
Explain the method of manufacturing and evaluation of floating tablets.
06
What is SOP? Explain SOP requirements in processing and packaging operation
05
Discuss the premises facility requirements as per GMP.
05
Q.4
Explain the classification of tablet tooling
06
Describe biodegradable and non-biodegradable polymers used in microcapsules
05
Explain quality control tests of hard and soft gelatin capsules
05
Q.5
Explain the term microsphere and give its importance
06
Give advantage and disadvantages of hard gelatin capsules
05
Discuss sugar coating in detail
05
Q. 6
Give the formulation and evaluation of dentifrice
06
Discuss regulatory requirements in pharmaceutical packaging
05
What is tamper evident package? Describe blister package.
05
Q.7
Discuss the evaluation parameters for mouth dissolving tablet
06
What is documentation? Describe batch manufacturing records
05
Write a brief note on shaving cream
05
GUJARAT TECHNOLOGICAL UNIVERSITY
B. Pharm SEMESTER-VIII EXAMINATION SUMMER 2017
Subject Code: 280002 Date: 29/04/2017
Subject Name: Pharmaceutical Technology-II
Time: 10:30 AM to 01:30 PM Total Marks: 80
Instructions:
1. Attempt any five questions.
2. Make suitable assumptions wherever necessary.
3. Figures to the right indicate full marks.
Q.1
Write note on in-process quality control test of tablet Mfg
06
Explain GMP with special ref. to personnel.
05
Give the difference between wet granulation and dry granulation
05
Q.2
Discuss the processing problems of tablets with remedies
06
Write a note on excipients and additives used in the capsule formulation
05
Classify cosmetics and write a short note on vanishing cream
05
Q.3
Explain the method of manufacturing and evaluation of floating tablets.
06
What is SOP? Explain SOP requirements in processing and packaging operation
05
Discuss the premises facility requirements as per GMP.
05
Q.4
Explain the classification of tablet tooling
06
Describe biodegradable and non-biodegradable polymers used in microcapsules
05
Explain quality control tests of hard and soft gelatin capsules
05
Q.5
Explain the term microsphere and give its importance
06
Give advantage and disadvantages of hard gelatin capsules
05
Discuss sugar coating in detail
05
Q. 6
Give the formulation and evaluation of dentifrice
06
Discuss regulatory requirements in pharmaceutical packaging
05
What is tamper evident package? Describe blister package.
05
Q.7
Discuss the evaluation parameters for mouth dissolving tablet
06
What is documentation? Describe batch manufacturing records
05
Write a brief note on shaving cream
05
Subjects
- agronomy and forestry of medicinal plants
- anatomy physiology & health education -ii
- anatomy, physiology and health education (aphe)
- applied mathematics (biostatistics)
- basic computer applications
- basic concepts of pharmacology and clinical pharmacy practice
- basics of computer applications
- bioavailability & therapeutic drug monitoring
- bioavailability and therapeutic drug monitoring
- biochemistry
- clinical pharmacy ii
- clinical pharmacy-i
- commerce of herbs and phytoconstitutents
- computer applications in drug discovery
- current advances in novel drug delivery systems
- cyber security
- disaster management
- dispensing pharmacy i
- dispensing pharmacy i and drug store management
- dispensing pharmacy ii and pharma industrial management
- dosage form design –i
- dosage form design- i
- dosage form design- ii
- dosage form design-i
- dosage form design-ii
- drug approval process
- environmental studies
- environmental toxicology and green audit
- food analysis
- forensic pharmacy
- forensic pharmacy-i
- genetic engineering and gene therapy
- green chemistry
- health education and community health
- herbal cosmetics
- hospital and community pharmacy
- hospital management and medical tourism
- hospital pharmacy, community pharmacy & forensic pharmacy
- hospital pharmacy, community pharmacy and dispensing pharmacy-ii
- human anatomy physiology
- human anatomy physiology and health education-ii
- human anatomy physiology-ii
- human anatomy, physiology and health education - i
- innovations in conventional drug delivery system
- instrumental and process validation
- intellectual property rights and patents
- medical writing and coding
- medicinal biochemistry
- nutraceuticals
- pathophysiology
- pharmaceutical analysis ii
- pharmaceutical analysis iii
- pharmaceutical analysis iv
- pharmaceutical analysis-i
- pharmaceutical analysis-ii
- pharmaceutical analysis-iv
- pharmaceutical chemistry – ii
- pharmaceutical chemistry – vi (organic chemistry – ii)
- pharmaceutical chemistry –viii (medicinal chemistry - ii)
- pharmaceutical chemistry iii
- pharmaceutical chemistry iv
- pharmaceutical chemistry vii
- pharmaceutical chemistry-i
- pharmaceutical chemistry-i (inorganic chemistry)
- pharmaceutical chemistry-ii (physical chemistry)
- pharmaceutical chemistry-iii (biochemistry – i)
- pharmaceutical chemistry-iv (organic chemistry-i)
- pharmaceutical chemistry-ix (medicinal chemistry-iii)
- pharmaceutical chemistry-v
- pharmaceutical chemistry-v (biochemistry-ii)
- pharmaceutical chemistry-vi (medicinal)
- pharmaceutical chemistry-vii
- pharmaceutical chemistry-viii
- pharmaceutical chemistry-x
- pharmaceutical chemistry-x (medicinal chemistry-iii)
- pharmaceutical engineering
- pharmaceutical engineering-ii
- pharmaceutical inorganic chemistry
- pharmaceutical marketing management
- pharmaceutical microbiology - i
- pharmaceutical microbiology & biotechnology i
- pharmaceutical microbiology &biotechnology- ii
- pharmaceutical microbiology and biotechnology - ii
- pharmaceutical organic chemistry
- pharmaceutical technology - i
- pharmaceutical technology – i
- pharmaceutical technology- ii
- pharmaceutical technology-i
- pharmaceutical technology-ii
- pharmaceutics-i
- pharmaceutics-ii
- pharmaceutivcal chemistry ix
- pharmacognosy iii
- pharmacognosy iv
- pharmacognosy vi
- pharmacognosy vii
- pharmacognosy vii (herbal formulations & complimentary therapies)
- pharmacognosy-i
- pharmacognosy-ii
- pharmacognosy-iii
- pharmacognosy-iv
- pharmacognosy-v
- pharmacognosy-v (plant bio technology)
- pharmacognosy-vi
- pharmacology -iii
- pharmacology & pharmacotherapeutics-ii
- pharmacology and pharmacotherapeutics - i
- pharmacology and pharmacotherapeutics - iii
- pharmacology and pharmacotherapeutics-iv
- pharmacology-i
- pharmacology-ii
- pharmacovigilance
- pharmacy practice
- physical pharmaceutics-ii
- physical pharmacy
- quality by design (qbd) and process analytical technology (pat)
- regulatory aspects of food and neutraceuticals
- remedial mathematics
- unit operation - i
- unit operation - ii