Exam Details
| Subject | pharmaceutical technology- ii | |
| Paper | ||
| Exam / Course | b.pharm | |
| Department | ||
| Organization | Gujarat Technological University | |
| Position | ||
| Exam Date | May, 2019 | |
| City, State | gujarat, ahmedabad |
Question Paper
Seat No.: Enrolment No.
GUJARAT TECHNOLOGICAL UNIVERSITY
B.PHARM SEMESTER- 8 EXAMINATION SUMMER -2019
Subject Code: 280002 Date: 08-05-2019
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
Define pharmaceutical package. Enlist the criteria for selection of package type and packaging material. Classify the packaging materials.
06
Give the evaluation test for closure as per IP. Write note on temper evident packaging.
05
Discuss regulatory requirements in pharmaceutical packaging.
05
Q.2
Differentiate between direct compression and wet granulation methods for tablet.
06
Define tablets. Give a brief account of processing problems and its remedies for tablets.
05
Enumerate specialized coating processes.
05
Q.3
Give a brief account on Cosmaceuticals.
06
Describe formulation aspects of baby care products.
05
Explain the popular cosmetic which contains Nitrocellulose as film former.
05
Q.4
Enlist methodologies of microencapsulation and discuss in detail coacervation phase separation method.
06
Discuss quality control parameters of soft gelatin capsules.
05
Define SOP. Describe content and format of SOP.
05
Q.5
Describe filling operation for hard gelatin capsules.
06
Briefly discuss the Good Manufacturing Practice for Pharmaceuticals.
05
Give the advantages of pharmaceutical validation. How will you perform validation of steam sterilizer?
05
Q. 6
Comment:
Plastic containers are more preferable than glass containers in Large Volume Parenterals.
Mannitol is used as diluent in chewable tablet.
Blooming and covering agents is added in face powder.
06
Explain and classification of tablet tooling.
05
Justify: Documentation is an essential part in GMP.
05
Q.7
Explain the formulation and evalution test on buccal tablets.
06
Describe biodegradable and non-biodegradable polymers used in microcapsules.
05
Write a note on blister and strip package.
05
GUJARAT TECHNOLOGICAL UNIVERSITY
B.PHARM SEMESTER- 8 EXAMINATION SUMMER -2019
Subject Code: 280002 Date: 08-05-2019
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
Define pharmaceutical package. Enlist the criteria for selection of package type and packaging material. Classify the packaging materials.
06
Give the evaluation test for closure as per IP. Write note on temper evident packaging.
05
Discuss regulatory requirements in pharmaceutical packaging.
05
Q.2
Differentiate between direct compression and wet granulation methods for tablet.
06
Define tablets. Give a brief account of processing problems and its remedies for tablets.
05
Enumerate specialized coating processes.
05
Q.3
Give a brief account on Cosmaceuticals.
06
Describe formulation aspects of baby care products.
05
Explain the popular cosmetic which contains Nitrocellulose as film former.
05
Q.4
Enlist methodologies of microencapsulation and discuss in detail coacervation phase separation method.
06
Discuss quality control parameters of soft gelatin capsules.
05
Define SOP. Describe content and format of SOP.
05
Q.5
Describe filling operation for hard gelatin capsules.
06
Briefly discuss the Good Manufacturing Practice for Pharmaceuticals.
05
Give the advantages of pharmaceutical validation. How will you perform validation of steam sterilizer?
05
Q. 6
Comment:
Plastic containers are more preferable than glass containers in Large Volume Parenterals.
Mannitol is used as diluent in chewable tablet.
Blooming and covering agents is added in face powder.
06
Explain and classification of tablet tooling.
05
Justify: Documentation is an essential part in GMP.
05
Q.7
Explain the formulation and evalution test on buccal tablets.
06
Describe biodegradable and non-biodegradable polymers used in microcapsules.
05
Write a note on blister and strip package.
05
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- 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