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Ustekinumab (Stelara) [Internet]. Ottawa (ON): Canadian Agency for Drugs and Technologies in Health; 2017 Apr.
Table 6Submission Quality
Yes/Good | Somewhat/Average | No/Poor | |
---|---|---|---|
Are the methods and analysis clear and transparent? | X | ||
Comments | None | ||
Was the material included (content) sufficient? | X | ||
Comments | None | ||
Was the submission well organized and was information easy to locate? | X | ||
Comments | None |
Table 7Authors’ Information
Authors of the pharmacoeconomic evaluation submitted to CDR | |||
---|---|---|---|
□ Adaptation of global model/Canadian model done by the manufacturer ⊠ Adaptation of global model/Canadian model done by a private consultant contracted by the manufacturer □ Adaptation of global model/Canadian model done by an academic consultant contracted by the manufacturer □ Other (please specify) | |||
Yes | No | Uncertain | |
Authors signed a letter indicating agreement with entire document | X | ||
Authors had independent control over the methods and right to publish analysis | X |
- ADDITIONAL INFORMATION - Ustekinumab (Stelara)ADDITIONAL INFORMATION - Ustekinumab (Stelara)
- EXECUTIVE SUMMARY - Glycerol Phenylbutyrate (Ravicti)EXECUTIVE SUMMARY - Glycerol Phenylbutyrate (Ravicti)
- EXCLUDED STUDIES - Ustekinumab (Stelara)EXCLUDED STUDIES - Ustekinumab (Stelara)
- PATIENT INPUT - Glycerol Phenylbutyrate (Ravicti)PATIENT INPUT - Glycerol Phenylbutyrate (Ravicti)
- INTERPRETATIONS AND KEY LIMITATIONS - Somatropin (Genotropin) (0.15 mg/day to 0....INTERPRETATIONS AND KEY LIMITATIONS - Somatropin (Genotropin) (0.15 mg/day to 0.3 mg/day)
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