Mark Warawa moved, — That Bill C-307 be amended by adding after line 17 on page 2 the following new clause:“3.2 The Minister of Health shall
(a) within three months after the coming into force of this Act, finalize the Department
of Health’s position paper on bis(2-ethylhexyl)phthalate in medical
devices;
(b) within 12 months after the coming into force of this Act, publish a document
concerning the labelling that is necessary to comply with the requirements of the
Medical Devices Regulations in relation to the risks inherent in medical devices
that contain bis(2-ethylhexyl)phthalate;
(c) within 24 months after the coming into force of this Act, require
the labelling of medical devices that contain bis(2-ethylhexyl)phthalate;
(d) facilitate the drafting by health professionals associations and
hospital associations of clinical practice guidelines respecting the use of medical
devices that contain bis(2-ethylhexyl)phthalate and to have the drafting of those
guidelines completed within 33 months after the coming into force of this Act;
(e) within 18 months after the coming into force of this Act, prepare a list of
medical devices that do not contain bis(2-ethylhexyl)phthalate that are sold in or
imported into Canada; and
(f) consider for priority review, applications for medical devices licences where
information obtained during the application process discloses that the medical
devices do not contain bis(2-ethylhexyl)phthalate.”
Debate arose thereon.