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0rganization
20, AVENUE APPIA-CHI211 GENEVA 27 - SWIIZERLAND - TET CENTML +41 22 791 2111-FAX CENTML r41 22 79131I1_IXWW,WHO JNr
' ^
017
Dear Mr Mathew,
Tlrank you for submitting the information request€d and for your voluntary pafticipation in this
procedure for conversion. The review ofyour company,s application for conversion
on:
r 004-011 - LIMITOR 5 CR
has been completed and it has been found to meet the criteria for conversion ro Prequalification and
is
acceptable, in principle, for procurement by uN and other international agencies and countries.
This conclusion is based on information available to wHo at the current tirne. i.e. the
information in the application for conversion and previous evaluations/reports. Please note, however, that
this decision may change based on new infomration that may become aviilable. Therefore,
ihe product
will now be included on the list ofvector control products, which are considered to be accentable. in
principle, for procurement by [lN organizations. This list is published by WHO at
http:/,/www.who. intlpq-vector-control/prequalifi ed-listslen/.
Please not€ that inclusion on the list cannot be construed as wHo approval or endorsement, and
nec
does not tually be procured irom the suppliers mentioned.
and
The list, ay not, funhermore, be used by the applicants,
manufacture cial or promotional purposes.
The applicants and the manufacturers ofprequarified products are required to comrnunicate to
wHo details ofany changes in manufacture or control that may have an impact on the safety, efficacy
and/or quality oflhe product.
ENCLS: (l)
Finally, I should like to draw your attention to the fact that the list will be reviewed and updated
at regularintervals. consequently, wHo could, at regular intervals, arrange for the products
included on
the list to be re-evaluated.
Yours sincerely,
'L?^r'o,G,J
Marion Law
Croup Lead, Vector Control Producrs
Prequalification Team
Regulation of Medicines and other Health Technoloeies