Public Minutes
Public Minutes
3 July
Time Agenda item Lead
(Dhaka)
09:00 Opening address WR Bangladesh on
behalf of the Regional
Director (TBC)
09:15 Speech from honourable State Minister, MOHFW, Dr. Rokeya Sultana
Bangladesh
Honourable State
Minister, MOHFW,
Bangladesh
09:25 Speech from honourable Minister of Health & Family Welfare, Dr. Samanta Lal Sen
Bangladesh
Honourable Minister
MOHFW, Bangladesh
09:40 Introduction of the participants, and update on countries not Chair and Secretariat
participating in this meeting
The meeting was opened by addresses from the Regional Director of WHO South-East Asia Regional
Office, Ms. Saima Wazed, read by the WHO representative in Bangladesh, Dr Bardan Jung Rana, the
Secretary of the Ministry of Health and Family Welfare (MOHFW), Mr. Md. Jahangir Alam, the
honourable State Minister, MOHFW, Dr. Rokeya Sultana, the honourable Minister of Health & Family
Welfare, Dr. Samanta Lal Sen, and a vote of thanks from Major General Mohammad Yousuf, Director
General, DGDA and Chair of the Assembly. The honourable guests welcomed the delegates of the
Assembly, and highlighted the importance of SEARN to strengthen health systems and achieve
universal health coverage through access to affordable, quality, safe and effective medical products.
The Assembly was informed by the Secretariat that:
the government of DPR Korea was not able to nominate participants for this meeting
WHO, as secretariat of SEARN, was not able to liaise with the government of Myanmar for this
meeting.
The Assembly was informed about the Latest global developments in medical products regulation in a
presentation from Dr Samvel Azatyan, covering the importance of reliance, Regulatory System
Strengthening activities, and WHO Listed Authorities (WLAs).
Dr Rajeev Singh Raghuvanshi and Dr Samvel Azatyan informed the Assembly about the 19th
International Conference of Drug Regulatory Authorities (ICDRA) which will be held in New Delhi,
India, from 14 to 18 October 2024, and invited SEARN Members to participate.
Dr Anil Chawla described the process of introduction of a new vaccines and the challenges in the
region, and highlighted the importance of reliance, streamlining regulatory processes, and
collaboration to ensure timely access to quality, safe and effective vaccines.
Dr Shanthi Pal informed the Assembly about the global actions from WHO to strengthen safety
surveillance of maternal and perinatal health, including the establishment of background rates of
adverse events of special interest to strengthen signal detection and assessment, and the
recommendations from ACSoMP on valproic acid. The participants noted the existence of resources in
the region which could be used to study and monitor the safety of medical products during
pregnancy.
Dr. Farhana Dewan shared her knowledge about the safety of medicines during pregnancy,
highlighting the specificities of this period and its challenges, and the shared responsibilities of all
actors to counsel patients with complete, accurate and current information on the risks and benefits
of medical products.
Dr. Syed Ghulam Mogni Mowla highlighted the criticality of addressing antimicrobial resistance, the
complexity of the challenges, and the leading role of the government of Bangladesh in this global
fight.
13:00 Coalition of interested Parties (CIP): update, support CIP members and All
provided, expectations and way forward participants
The secretariat provided an overview of the current status of the SEARN CIP. CIP members presented
to the Assembly the support provided during the 2023-2024 work plan. The Assembly expressed its
The Assembly was informed that since its last meeting in July 2023, there have been three meetings
of the Steering group, 15 Meetings of the 5 Working groups (three each), and 58 meetings of the 12
drafting groups. There were also one exceptional meeting on the minimum information required for
reliance and one optional information meeting on the SEARN Competency framework. Six surveys
have been finalised.
The Assembly highlighted the importance of adequate representation of NRAs in the Network to
ensure it has the power to take decisions on the issues discussed in all SEARN Members. SEARN
Members noted that relevant authorities can participate in any relevant working groups and drafting
groups, and that the secretariat can facilitate invitation to other authorities when requested by a
Member. Informed by a survey and further discussions in the Steering group on 2 July 2024 and
during the Assembly, the Assembly agreed that the following NRAs should be invited in the following
meetings of the Assembly:
Bhutan: National Medical Product Testing Laboratory (1 representative)
India: Indian Pharmacopoeia Commission (1 representative), State/UT Drug Control
Authorities (2 representatives to be selected by the NRA)
Sri Lanka: Medical Research Institute (vaccines department) (1 representative)
Thailand: Department of Medical Sciences (1 representative)
In addition, the Assembly requested the SEARN secretariat to invite the relevant authorities to
nominate representatives towards establishing a working group 6 dedicated to traditional products.
The Assembly adopted the results of the 2023-2024 exercise and the proposed changes in the
Monitoring and evaluation framework. While some positive impact was observed, the Assembly
noted that more time and efforts are required to achieve the goals set by the strategies.
Dr Sabine Strauss presented perspectives and experience from the European Union regarding the
safety of medicines during pregnancy, covering EU Guidance Good Vigilance Practice regarding Risk
Management Plans and risk minimisation tools and Pregnancy Prevention Plans. The presentation
highlighted the aims of the different tools, examples, as well as the challenges in implementing these
and the importance of measuring impact.
Considering the SEARN strategies and workplan, as well as the contributions made during the sessions
dedicated to safe medicines during pregnancy, the Assembly recommended that SEARN:
Develop a domain in its competency framework to support NRAs in ensuring safe medicines
during pregnancy (AP1)
Pilot the regional mechanism for recommendations on risk management with valproate
(AP15)
Include pregnancy adverse events in the priority list for monitoring /detection at the regional
level (AP16)
WG1 Quality
The Assembly adopted the proposed outputs (AP8, AP9, AP14) presented by the Chair of the working
group, and agreed on the publication of public summaries, including:
AP8: the highlights from the Regional hybrid workshop on the optimal use of reference
standards
AP9: the template of a practical guide to testing in a country template
AP14: the highlights from the 3 meetings and the recommendations to WHO, SEARN
Members and the Assembly.
The Assembly invited SEARN Members, partners and WHO to continue their efforts in developing and
implementing reliance.
WG3 Vigilance
The Assembly adopted the proposed outputs (AP15, AP16) presented by the Chair of the working
group, and agreed on the publication of public summaries, including:
AP16: the list of priority medicines
The Assembly adopted the proposed 2024-2025 Workplan, and amended and adopted the proposed
rapporteurs and drafting group members.
The secretariat provided the Assembly with a summary of the main decisions made during this
meeting.
The meeting was concluded by Chair of the Assembly, who thanked the speakers and attendees for
their active participation in this meeting and congratulated the Assembly for having successfully
achieved all the objectives of the meeting. The Chair appreciated the efforts from all members of the
drafting groups, working groups, Steering group, Assembly and the secretariat over the past year,
welcomed the new work plan and congratulated Bhutan and Nepal as the hosts of the next meetings
of the Assembly. The secretariat, on behalf of the Members of SEARN, thanked the Government of
Bangladesh, and especially Ministry of Health and Family Welfare and the Directorate General of Drug
Administration (DGDA), as well as the WHO country office of Bangladesh for their support and the
successful organization of the meeting.