Consultation record
Submissions accepted in part — page 2
Part of the submission is accepted and part is not. The secretariat response states which part is which and on what ground the remainder was declined.
Submissions
390 documents · page 2 of 13
Table 1. Submissions with this disposition, on this page.
| Reference | Consultation | Respondent | Point raised |
|---|---|---|---|
| DRAFT-WEIGHT-REGAI/012 | Draft synthesis: weight change after discontinuation of an incretin… | Dr Matthias Wintringham industry | A sponsor trial meeting the eligibility criteria was excluded |
| DRAFT-NETWORK-TRAN/002 | Draft methodological review: transitivity in the incretin network | Dr Vasilisa Immelmann | Regulatory assessment documents were not searched |
| DRAFT-NETWORK-TRAN/003 | Draft methodological review: transitivity in the incretin network | Dr Yaa Kettlewell | Statistical heterogeneity is treated as though it measured clinical heterogeneity |
| DRAFT-NETWORK-TRAN/004 | Draft methodological review: transitivity in the incretin network | Eamon Sandringham-Adu | The review protocol is described but its registration record is not linked |
| DRAFT-CONFLICTS-PO/007 | Draft conflicts-of-interest policy | Georgiana Zimmerthal | The materiality threshold for a declarable holding is set too high |
| DRAFT-CONFLICTS-PO/008 | Draft conflicts-of-interest policy | Ignatius Erlingsson | A four-week window is too short for a respondent without institutional support |
| DRAFT-CONFLICTS-PO/009 | Draft conflicts-of-interest policy | Dr Rurik Haverkamp-Diallo | Funding should not be accepted from any party the Institute assesses |
| DRAFT-FUNDING-POLI/005 | Draft funding and sponsorship policy | Ivo Mountstephen | References should carry a persistent identifier for every cited source |
| DRAFT-FUNDING-POLI/007 | Draft funding and sponsorship policy | Ignatius Erlingsson | A four-week window is too short for a respondent without institutional support |
| DRAFT-CITATION-POL/008 | Draft citation policy | Dr Vasilisa Sandringham-Adu | The materiality threshold for a declarable holding is set too high |
| DRAFT-PROGRAMME-RE/002 | Draft policy: labelling of Institute-constructed programme records | Ms Rhiannon Okoye-Vandergraaf | The document is unreadable without specialist training |
| DRAFT-PROGRAMME-RE/006 | Draft policy: labelling of Institute-constructed programme records | Kamila Ubertini | A four-week window is too short for a respondent without institutional support |
| DRAFT-PROGRAMME-RE/009 | Draft policy: labelling of Institute-constructed programme records | Dr Wojciech Kaltenbach-Mensah | The secretariat answers submissions and is not itself named |
| DRAFT-PROGRAMME-RE/011 | Draft policy: labelling of Institute-constructed programme records | Dr Vasilisa Immelmann | A party criticised in an assessment should have a right of reply |
| DRAFT-PROGRAMME-RE/012 | Draft policy: labelling of Institute-constructed programme records | Dr Emiliana Ollerenshaw | Funding should not be accepted from any party the Institute assesses |
| DRAFT-ENDOTOXIN-ST/002 | Draft standard: bacterial endotoxin testing of peptide presentations | Dr Quentin Zimmerthal | Nothing in the standard addresses transfer of the method between laboratories |
| DRAFT-ENDOTOXIN-ST/006 | Draft standard: bacterial endotoxin testing of peptide presentations | Bertrand Ollerenshaw industry | The additional determinations required would materially increase release testing cost |
| DRAFT-ENDOTOXIN-ST/007 | Draft standard: bacterial endotoxin testing of peptide presentations | Thaddeus Isaksen-Balogun | Point estimates are given without an interval |
| DRAFT-ENDOTOXIN-ST/008 | Draft standard: bacterial endotoxin testing of peptide presentations | Dr Jolanta Uttridge | Nothing addresses the container the material was held in |
| DRAFT-ENDOTOXIN-ST/012 | Draft standard: bacterial endotoxin testing of peptide presentations | Dr Hortensia Hollingworth | Nothing requires a laboratory to demonstrate ongoing performance |
| DRAFT-ANALYTICAL-S/003 | Draft scope of the analytical and methodological standards series | Eamon Sandringham-Adu | References should carry a persistent identifier for every cited source |
| DRAFT-ANALYTICAL-S/004 | Draft scope of the analytical and methodological standards series | Amara Vandergraaf | Defined terms are defined in a glossary the reader has to know exists |
| DRAFT-ANALYTICAL-S/009 | Draft scope of the analytical and methodological standards series | Dr Marisol Dunmore-Ekpo | An index organised by certainty invites comparison between ratings that are not comparable |
| DRAFT-GLP1-OBESITY/002 | Draft synthesis: glucagon-like peptide-1 receptor agonists for weight… | Dr Yaa Kettlewell | The axis of the forest plot exaggerates a small difference |
| DRAFT-GLP1-OBESITY/005 | Draft synthesis: glucagon-like peptide-1 receptor agonists for weight… | Ms Rhiannon Okoye-Vandergraaf | The document is unreadable without specialist training |
| DRAFT-GLP1-OBESITY/007 | Draft synthesis: glucagon-like peptide-1 receptor agonists for weight… | Professor Bartolomeu Nkosi-Lindegaard | Regulatory assessment documents were not searched |
| DRAFT-GLP1-OBESITY/008 | Draft synthesis: glucagon-like peptide-1 receptor agonists for weight… | Dr Liesbeth Nordhagen industry | A sponsor trial meeting the eligibility criteria was excluded |
| DRAFT-GLP1-OBESITY/009 | Draft synthesis: glucagon-like peptide-1 receptor agonists for weight… | Quentin Whitmarsh-Obi | The review protocol is described but its registration record is not linked |
| DRAFT-GLP1-OBESITY/013 | Draft synthesis: glucagon-like peptide-1 receptor agonists for weight… | Dr Oisín Rautavaara | The choice of effect measure is not justified and changes the appearance of the result |
| DRAFT-LEAN-MASS-SC/001 | Draft scoping review: change in lean mass during pharmacologically… | Ms Rhiannon Okoye-Vandergraaf | Patient-reported outcomes are collected by the trials and not reported by the review |
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