Round 2

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Across
  1. 4. What is an individual or pharmaceutical company, governmental agency, academic institution, private organization, or other organisation called who takes responsibility for and initiates a BA or BE (in vivo or in vitro) study
  2. 10. The ____ diameter of an aerosol particle is equal to the diameter of a sphere of unit density whose gravimetric settling velocity is the same.
  3. 14. What is the term used for the remainder of the discharge from the inhaler that is inhaled into the remainder of the respiratory tract?
  4. 15. ____ is performed to confirm that the amount of drug discharged from the product and recovered from the mouthpiece/nosepiece adapter, induction port, and after-filter of the cascade impacted is within an acceptable range of the target-delivered label claim?
  5. 16. Which is the medium that is primarily intended for the culture of anaerobic bacteria?
  6. 18. A component or entity that may come into contact with a tertiary packaging component during the distribution, storage, transportation of the packaged article is known ____ component.
Down
  1. 1. What is the name of Cipla’s flagship respiratory initiative that has broadened its footprint in the UAE?
  2. 2. What is the API in Cipla’s advanced IV antibiotic drug ZEMDRI?
  3. 3. A column that has no packed solid support and in which the liquid stationary phase is deposited or chemically bonded to the inner surface of the column, is known as a ___ column.
  4. 5. _____ is the process of acquiring and evaluating data that establishes the biological safety of an individual degradation product or a given degradation profile at the level(s) specified.
  5. 6. The applicant’s QMS (quality management system) should include the design and implementation of efficient protocols including tools and procedures for study conduct to support participant’s rights, _____ and well-being and the reliability of study results.
  6. 7. Which glucagon-like peptide-1 (GLP-1) has been announced by Eli Lily and Cipla in an agreement to distribute in India under the Yurpeak brand?
  7. 8. In particular, analytical procedures should be validated to demonstrate ___ for the specified and unspecified degradation products.
  8. 9. Which manufacturing process step poses risk when nitrous acid is used for azide decomposition?
  9. 11. Under the agreement with Pfizer, which non-steroidal anti-inflammatory drug (NSAId) does Cipla have the sole right to distribute and sell in India?
  10. 12. For a ____, the core formulation(s) of the additional strength(s) should be qualitatively the same as that of the biobatch strength(s).
  11. 13. Cipla has exclusive rights in India for ____ inhalation powder, a non-injectable, rapid-acting inhaled insulin developed by the American company Mankind.
  12. 16. _____ assays serve multiple purposes in the characterization of protein products. These tests complement physiochemical analyses and are a quantifiable measure of the function of the protein product.
  13. 17. A packaging component that is in direct contact with, or may come into direct contact with the article, is known as ______ packaging component.