PMPRB HDAP Meeting Dates & Submission Deadlines

The following table provides the submission deadlines for the HDAP meetings in 2020:

HDAP Meeting Date Filing Deadlines
Product Monograph (1) Submission (2)
February 10, 2020 November 14, 2019 December 5, 2019
May 25, 2020 January 16, 2020 February 13, 2020
September 21, 2020 June 4, 2020 July 2, 2020
November 23, 2020 August 6, 2020 September 10, 2020
  1. One (1) copy of product monograph or information similar to that included in a product monograph (if product has not yet been approved for sale in Canada) and the proposed level of therapeutic improvement

  2. One (1) electronic copy of patentee submission

The following table provides the submission deadlines for the HDAP meetings in 2019:

HDAP Meeting Date Filing Deadlines
Product Monograph (1) Submission (2)
February 25, 2019 November 1, 2018 November 29, 2018
May 27, 2019 January 10, 2019 February 14, 2019
September 30, 2019 May 23, 2019 June 27, 2019
November 25, 2019 August 1, 2019 September 5, 2019
  1. One (1) copy of product monograph or information similar to that included in a product monograph (if product has not yet been approved for sale in Canada) and the proposed level of therapeutic improvement

  2. One (1) electronic copy of patentee submission

The following table provides the submission deadlines for the HDAP meetings in 2018:

HDAP Meeting Date Filing Deadlines
Product Monograph (1) Submission (2)
February 27, 2018 November 7, 2017 December 12, 2017
May 7, 2018 January 11, 2018 February 15, 2018
September 24, 2018 May 10, 2018 June 7, 2018
November 26, 2018 July 26 2018 August 23, 2018
  1. One (1) copy of product monograph or information similar to that included in a product monograph (if product has not yet been approved for sale in Canada) and the proposed level of therapeutic improvement

  2. One (1) electronic copy of patentee submission

The following table provides the submission deadlines for the HDAP meetings in 2017:

HDAP Meeting Date Filing Deadlines
Product Monograph (1) Submission (2)
February 27, 2017 November 14, 2016 December 8, 2016
May 29, 2017 January 19, 2017 February 16, 2017
September 18, 2017 May 25, 2017 June 22, 2017
December 4, 2017 July 27 2017 August 24, 2017
  1. One (1) copy of product monograph or information similar to that included in a product monograph (if product has not yet been approved for sale in Canada) and the proposed level of therapeutic improvement

  2. One (1) electronic copy of patentee submission

The following table provides the submission deadlines for the HDAP meetings in 2016:

HDAP Meeting Date Filing Deadlines
Product Monograph (1) Submission (2)
February 29, 2016 November 12, 2015 December 10, 2015
May 2, 2016 January 7, 2016 February 4, 2016
September 12, 2016 May 12, 2016 June 9, 2016
November 28, 2016 July 21 2016 August 18, 2016
  1. One (1) copy of product monograph or information similar to that included in a product monograph (if product has not yet been approved for sale in Canada) and the proposed level of therapeutic improvement

  2. One (1) electronic copy of patentee submission

The following table provides the submission deadlines for the HDAP meetings in 2015:

HDAP Meeting Date Filing Deadlines
Product Monograph (1) Submission (2)
February 9, 2015 October 30, 2014 November 27, 2014
May 4, 2015 January 15, 2015 February 19, 2015
September 14, 2015 May 14, 2015 June 18, 2015
November 30, 2015 July 23 2015 August 20, 2015
  • One (1) copy of approved Product Monograph
    • If not approved the draft product monograph submitted to Health Canada or a document with similar information such as an approved monograph from another jurisdiction (e.g., US, Europe)
  • EIGHT (8) copies of patentee (manufacturer) submission

The following table provides the submission deadlines for the HDAP meetings in 2014:

HDAP Meeting Date Filing Deadlines
Product Monograph (1) Submission (2)
February 10, 2014 October 18, 2013 November 18, 2013
May 12, 2014 January 20, 2014 February 18, 2014
September 15, 2014 May 26, 2014 June 25, 2014
November 10, 2014 July 18, 2014 August 18, 2014
  • One (1) copy of approved Product Monograph
    • If not approved the draft product monograph submitted to Health Canada or a document with similar information such as an approved monograph from another jurisdiction (e.g., US, Europe)
  • EIGHT (8) copies of patentee (manufacturer) submission