Questions and responses 41st Parliament, 2nd session October 16, 2013, to August 2, 2015

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Historical information
The information shown below relates to a prior session.

Q-245

41-2
October 16, 2013, to August 2, 2015

Q-245

41st Parliament, 2nd session
Asked by
Date asked
January 28, 2014
Answered
March 24, 2014
With regard to Marihuana for Medical Purposes Regulations: (a) how many applications to become licensed producers have been received by Health Canada; (b) from which municipality or township does each application come; (c) how many applications have been approved and in what municipality or township are they located; (d) what has been the cost to Health Canada to implement the new regulations; (e) will there be sufficient supply of medical marihuana as of April 1, 2014 to fulfill the medical needs of current patients and, if not, how will Health Canada ensure that there is no interruption in supply; and (f) once a patient submits their prescription or current license to grow marihuana at home to a licensed producer, will the patient be permitted to switch to a different producer if they find a more competitive price?
Historical information
The information shown below relates to a prior session.

Q-948

41-2
October 16, 2013, to August 2, 2015

Q-948

41st Parliament, 2nd session
Asked by
Date asked
January 27, 2015
Answered
March 13, 2015
With regard to Health Canada’s regulation of medical marijuana: (a) for the seven-step application process for producers, (i) how many applications have been received, (ii) how many are at each stage, (iii) what is the average time required to complete each stage since the program began, (iv) on average, how long have applications, presently in process at each stage, been at that stage, (v) how many staff process applications, (vi) of those staff identified in (v), how many have degrees outside the health sciences, (vii) of those staff identified in (v), how many have formal education in finance, (viii) for how many applicants at each stage is the Department aware of non-compliance with applicable federal, provincial, territorial, and municipal legislation, regulations and bylaws, (ix) are media reports about applicants reviewed, (x) what fees are charged to applicants, (xi) what are the costs of processing an application; (b) what is the production capacity of licensed vendors; (c) how many patients are registered to purchase medical marijuana; and (d) what is the total quantity of medical marijuana required for registered patients?
Historical information
The information shown below relates to a prior session.

Q-889

41-2
October 16, 2013, to August 2, 2015

Q-889

41st Parliament, 2nd session
Asked by
Date asked
December 8, 2014
Answered
January 26, 2015
With regard to Health Canada and drug shortages: (a) what is the compliance rate with the voluntary drug-shortage reporting recommendations; (b) what communications has the Department received from concerned health care providers, pharmacists, patients and caregivers related to drug shortages; and (c) what actions has the Department undertaken to respond to these concerns?
Historical information
The information shown below relates to a prior session.

Q-1020

41-2
October 16, 2013, to August 2, 2015

Q-1020

41st Parliament, 2nd session
Asked by
Date asked
February 4, 2015
Answered
March 20, 2015
With regard to Health Canada and the regulation of pharmaceutical manufacturing companies for the last ten years: (a) how many companies inspected in Canada have received a “proposal to suspend” letter, broken down by year; (b) how many companies inspected in Canada have received an “immediate suspension,” broken down by year; (c) how many companies inspected in Canada that were not sent a “proposal to suspend” letter or subject to a suspension has Health Canada worked with following an inspection to bring about compliance, broken down by year; (d) how many companies inspected in Canada have been subject to a re-inspection within six months, broken down by year; (e) how many companies inspected internationally have received a “proposal to suspend” letter, broken down by year; (f) how many companies inspected internationally have received an “immediate suspension,” broken down by year; (g) how many companies inspected internationally that were not sent a proposal to suspend letter or subject to a suspension has Health Canada worked with following an inspection to bring about compliance, broken down by year; (h) how many pharmaceutical manufacturing companies inspected internationally have been subject to a re-inspection within six months, broken down by year; (i) how many Import Alerts has Health Canada issued with regard to non-compliant health products, broken down by year; (j) which companies have been subject to an Import Alert; (k) how many voluntary quarantine requests has Health Canada issued, broken down by year; (l) which companies have been subject to a voluntary quarantine request; (m) how many “Notice of Intent to Suspend” letters have been issued to clinical trials, broken down by year; (n) how many “immediate suspensions” has Health Canada issued to clinical trials, broken down by year; (o) how many complaints have been received regarding off-label prescriptions of drugs, broken down by year; and (p) how many cases has Health Canada referred to the Public Prosecution Service of Canada for off-label prescriptions of drugs?
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