000 01357nam  2200325zi 4500
0019.919266
003CaOODSP
00520230313123350
006m     o  d f      
007cr |||||||||||
008230118t20232023onc     o    f000 0 eng d
020 |a9780660471624
040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH164-346/2023E-PDF
24500|aGuidance document : |bconduct and analysis of comparative bioavailability studies.
264 1|aOttawa, ON : |bHealth Canada = Santé Canada, |c2023.
264 4|c©2023
300 |a1 online resource (35 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
500 |aIssued also in French under title: Ligne directrice : conduite et analyse des études de biodisponibilité comparatives.
500 |a"Date Adopted: 2012/02/08. Revised Date: 2023/01/30. Effective Date: 2018/09/01 (for submissions filed on or September 1, 2018)."
650 0|aDrugs|xTesting|xGovernment policy|zCanada.
650 0|aDrugs|xBioavailability|zCanada.
7101 |aCanada. |bHealth Canada, |eissuing body.
77508|tLigne directrice : |w(CaOODSP)9.919268
795 |tGuidance document |w9.852787
85640|qPDF|s636 KB|uhttps://publications.gc.ca/collections/collection_2023/sc-hc/H164-346-2023-eng.pdf