Food and Drug Regulations
Version of section C.04.102 from 2006-03-22 to 2018-04-03:
C.04.102 Upon written request from the Director every fabricator and packager/labeller shall submit with respect to each lot of virus or rickettsial vaccine, when ready for sale, detailed protocols of sterility, safety, identity, potency, and of any other tests required by these Regulations.
- SOR/97-12, s. 63
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