Name: Steffany Joy M.

Desamito

Group: 4

Dosage Form Physical Test Chemical Test

1. Tablet a. Disintegration testing a. Dissolution Test

b. Friability testing b. Content Uniformity Test
c. Hardness testing c. Assay Of Active Ingredients
2. Capsules a. Disintegration testing a. Dissolution test
b. Weight variation b. Content uniformity test
c. Softgel hardness c. Stability Test Using “Jar Test”

3. Emulsions a. Accelerated stability testing a. Conductivity test

b. Dilution test b. Phase inversion test
c. Cobalt chloride test c. Stability test
a. Oral solutions and a. Rheology testing a. Chromatographic method
suspensions b. Pourability test for stability
c. Particle containment test b. Drug degradation test
c. Dissolution test
b. Powders and granules for oral a. Density test a. Potency test
solution and suspensions b. Photo microscopic examination b. Drug content uniformity
c. Flowability test c. Stability test using
chromatographic method
c. Nasal sprays d. Clarity test a. Pump delivery test
e. Droplet size distribution test b. Degradation test
f. pH Value test c. Spray content uniformity test
d. Topical, ophthalmic And a. Packaging material test a. Isotonicity test
optic preperations b. Viscosity test b. Hygroscopicity test
c. Specific gravity test c. Test for dehydration

d. Suppositiories a. Melting range test a. Dissolution test

b. Visual examination (color, b. Content uniformity
shape) c. In vitro evalution
c. Crushing test
d. Parenterals a. Package integrity leak test a. Sterility test
b. Clarity test b. Uniformity of dosage units
c. Test for volume of liquid c. Antimicrobial effectiveness
testing

Injections and Implanted Drug Products (Parenterals)—Product Quality Tests. (2016). Retrieved from
https://www.uspnf.com/sites/default/files/usp_pdf/EN/USPNF/revisions/gc_1_rb_notice.pdf

Quality control of suppositories. (n.d.). Retrieved from

https://www.pharmpress.com/files/docs/samplechapter.pdf

Uddin, M. S., Mamun, A. A., Rashid, M., & Asaduzzaman, M. (2015). British Journal of Pharmaceutical Research.
British Journal of Pharmaceutical Research.

Zografi, G. (n.d.). Physical stability assessment of emulsions and related disperse system.
1. Friability Test

 Friability testing is used to test the durability of tablets during packing processes and transit. This involves repeatedly
dropping a sample of tablets over a fixed time, using a rotating drum with a baffle. The result is inspected for broken
tablets, and the percentage of tablet mass lost through chipping.
