News

December 2016

Revision of PIC/S GMP Guide (PE 009-13)

Geneva, 22 December 2016: the following Chapters of the PIC/S GMP Guide have been revised:

  • Chapter 1 on “Quality Management” (which has become “Pharmaceutical Quality Systems”); 
  • Chapter 2 on “Personnel”;
  • Chapter 6 on “Quality Control”; 
  • Chapter 7 on “Contract Manufacture and Analysis” (which has become “Outsources Activities”).

The revised Chapters 1, 2, 6 & 7 of the PIC/S GMP Guide are based on the equivalent Chapters of the EU GMP Guide with some minor differences in terms of language. Chapters 1, 2 & 7 have been aligned to ICH Q10 and the principles of “Pharmaceutical Quality System” have been integrated. A section on consultants has been added in Chapter 2. The scope of Chapter 7 has been expanded beyond the scope of “contract manufacture and analysis”. Both Chapters 1 and 7 have been renamed to reflect the changes. In Chapter 6, all sections have been reviewed and amended and a new section on “Technical transfer of testing methods” has been added.

The revision has been successfully completed by the PIC/S Sub-Committee on the Harmonisation of GM(D)P, led by Paul Gustafson (Canada/RORB). The revised GMP Guide (PE 009-13) will enter into force on 1st January 2017. All non-EEA Participating Authorities of PIC/S (and Applicants) have been invited to transpose the revised Chapters of the PIC/S GMP Guide into their own GMP Guides.

To download the revised GMP Guide (PE 009-13), please consult the page “Publications” or click on the link below:

May 2019

PIC/S meetings in Geneva, Switzerland, 8-10 April 2019

Geneva, 21 May 2019: the PIC/S Committee met on 9-10 April 2019 in Geneva (Switzerland), preceded by a meeting of the PIC/S Executive Bureau on 8-9 April 2019.

The press release regarding these meetings is available in newsletter format here or can be downloaded in pdf format from the link below:

May 2019

2019 PIC/S Seminar (Toyama, Japan)

Geneva, 20 May 2019: Registrations for the 2019 PIC/S Seminar on "Quality Assurance of Sterile Medicinal Products - PIC/S GMP Guide Annex 1" (Toyama, 13-15 November 2019) are now open (for Medicines Regulatory Authorities only).

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Seminar 2019 logo

The 2019 PIC/S Annual Seminar on "Quality Assurance of Sterile Medicinal Products - PIC/S GMP Guide Annex 1" will be hosted by Japan's Ministry of Health, Labour and Welfare (MHLW) and Pharmaceuticals and Medicinal Devices Agency (PMDA) in Toyama (Japan) from 13-15 November 2019.

The Seminar will focus on Quality Assurance of Sterile Medicinal Products - PIC/S GMP Guide Annex 1 and will consist of interactive discussions, presentations and workshops. It will be an ideal opportunity for both novice and experienced inspectors to enhance their inspection skills through knowledge sharing and discussion. This Seminar is intended to provide a further understanding of PIC/S GMP Guide Annex 1 based on issues discussed during its ongoing revision and through a case study of sterility assurance. The Seminar will also allow participants to acquire skills on how to make risk based decisions during GMP inspections. Workshops will be supported by the use of videos of practical manufacturing operations in order to stimulate active discussions.

Registrations to the PIC/S Seminar 2019 are now open (for Medicines Regulatory Authorities only).

For more information and registration click here

March 2019

Bangladesh applies for PIC/S pre-accession

Geneva, 5 March 2019: On 26 February 2019, Bangladesh's Directorate General of Drug Administration (DGDA) applied for PIC/S pre-accession. The Rapporteurs will be appointed at the next PIC/S Committee meeting in Geneva (Switzerland) on 9-10 April 2019.

November 2018

Focused stakeholders consultation on revised draft PIC/S guidance on Good Practices for Data Management and Integrity in Regulated GMP/GDP Environments

Geneva, 30 November 2018: a revised Draft PIC/S Guidance on Good Practices for Data Management and Integrity in Regulated GMP/GDP Environments (PI 041-1 (Draft 3)) has been prepared by the PIC/S Working Group on Data Integrity, co-led by Australia / TGA and UK / MHRA.

The purpose of the guidance is to serve to outline the position an inspector would adopt during the inspection of GDP/GMP facilities and is designed to facilitate a harmonised approach to the inspection, including reporting in regards to data management and integrity. A first draft (PI 041-1 (Draft 2)) was published by PIC/S on a trial basis in August 2016. Following feedback received from PIC/S Participating Authorities during its 6-month implementation trial-period, the draft of this guidance has been updated and expanded by the Working Group.

The document (PI 041-1 (Draft 3)) is subject to a focused stakeholder consultation seeking substantive comments from trade and professional associations on specific questions relating to the proportionality, clarity and implementation of the guidance requirements. In parallel to this stakeholder consultation, the new draft will be applied by PIC/S Participating Authorities on a trial basis for a new implementation trial period.

The consultation period will last 3 months and run from 30 November 2018 to 28 February 2019.

To submit feedback, please provide feedback exclusively on the dedicated template available on the websites of the below associations and submit by e-mail with subject line "PIC/S Focused Public Consultation – Data Management and Integrity" to one of the following associations which will collect and compile responses. Stakeholders should only reply once.

To download the consultation document (PI 041-1 (Draft 3)) please consult the page “Publications” or click on the link below:

October 2018

PIC/S events in Chicago, United States, 24-28 September 2018

Geneva, 31 October 2018: the PIC/S Committee met on 24-25 September 2018 in Chicago, Illinois (USA). The meeting was followed by the PIC/S annual training Seminar on 26-28 September 2018. The topic of the seminar was "Management of Risk Through the Product Life-Cycle".

The press release regarding these events is available in newsletter format here or can be downloaded in pdf format from the link below: