This article has been
cited by other articles in ScienceCentral.
Abstract
Background
The Korea Expert Committee on Immunization Practices (KECIP) is a key advisory body the government to develop guidelines and provide technical advisory activities on immunization policies in Korea. A recent policy study, inspired by global best practices, aims to enhance KECIP's functionality for providing timely and transparent recommendations in the face of evolving vaccine science and emerging infectious diseases like COVID-19.
Methods
This study reviewed the current status of KECIP and collected expert opinions through surveys and consultations. Among the 40 panel members who were surveyed, 19 responded to a questionnaire specifically designed to assess the potential areas of improvement within KECIP.
Results
The majority of respondents favored maintaining the current member count and emphasized the need for a subcommittee. Opinions varied on issues such as the length of KECIP’s term, the representation of vaccine manufacturers’ perspectives, and the chairperson’s role. However, there was a consensus on the importance of expertise, transparency, and fair proceedings within the committee.
Conclusion
This study underscores the pivotal role of KECIP in shaping national immunization policies, emphasizing the necessity for informed guidance amidst evolving vaccine science and emerging infectious diseases. Furthermore, it stressed the importance of enhancing KECIP’s capacity to effectively address evolving public health challenges and maintain successful immunization programs in South Korea.
Keywords: Vaccine, Immunization, Evidence, Policy, Korea
INTRODUCTION
The Korea Expert Committee on Immunization Practices (KECIP), operating under the Infectious Disease Control Committee within the Korea Disease Control and Prevention Agency (KDCA), plays a vital advisory role in shaping immunization policies.
1 KECIP was established under Article 10-2 of the Infectious Disease Prevention Act and Article 3-3 of its Enforcement Decree, along with its 15 sub-committees, was constituted to develop guidelines for the prevention and management of vaccine-targeted infectious diseases and address key vaccine-related issues in Korea.
2 The KECIP has been served as an advisory body for the management of vaccine-targeted infectious diseases, with the primary objectives of designating and revoking infectious diseases requiring vaccination, establishing criteria for vaccination implementation, methods, policies for vaccine-targeted infectious disease management, and eradication plans.
Given the increasing complexities of vaccine science and emerging infectious diseases, such as coronavirus disease 2019 (COVID-19), there is a pressing need to enhance the functions and procedures of KECIP. This enhancement is imperative to provide timely, objective, and transparent recommendations.
3 To address this, a policy study was conducted, reviewing the current status of KECIP and similar committees worldwide, consulting domestic and international experts, and examining the operations of renowned committees, including the Strategic Advisory Group of Experts on Immunization and the US Advisory Committee on Immunization Practices. This study aimed to propose improvements to KECIP based on the findings collected from surveys and expert consultations.
METHODS
This study targeted the expert advisory panel of KECIP. Participation in the survey was solicited via e-mail from 40 experts identified by the KDCA, 19 of whom participated in the survey. The data were collected through an online survey conducted between January 15th and 19th, 2024.
The survey questionnaire developed by the authors was modified based on input from an infectious disease specialist and the head of the relevant department within the KDCA. The questionnaire comprised 47 multiple-choice questions aimed at improving KECIP across nine key topics (
Table 1): 1) Composition and structure of KECIP (5 items), 2) Submission of agenda to KECIP (3 items), 3) Preparation of materials and time for agenda deliberation by KECIP members (12 items), 4) Proposal of opinions from the perspective of vaccine manufacturers, citizens, and patients at KECIP meetings (7 items), 5) Impact of decisions made by KECIP (3 items), 6) Selection of expert committee members of KECIP (6 items), 7) Selection and role of the KECIP chairperson (4 items), 8) Role of committee members at KECIP meetings (3 items), and 9) Disclosure of results of KECIP meetings (4 items). The Korean questionnaire is presented in
Supplementary Data 1.
Table 1
Summary of the survey on the improvement of the KECIP

|
Contents of questionnaire |
Strongly disagree |
Disagree |
Neutral |
Agree |
Strongly agree |
|
1. Composition and structure of KECIP |
|
|
|
|
|
|
1-1. The current number of members of KECIP (15 people) is adequate. |
1 (5.3) |
1 (5.3) |
3 (15.8) |
11 (57.9) |
3 (15.8) |
|
1-2. The current term of office for KECIP (2 yr) is appropriate. |
1 (5.3) |
6 (31.6) |
4 (21.1) |
6 (31.6) |
2 (10.5) |
|
1-3. The operation of permanent subcommittees is necessary. |
0 |
2 (10.5) |
1 (5.3) |
6 (31.6) |
10 (52.6) |
|
1-4. The subcommittee must be able to submit meeting agendas related to vaccines under development or the introduction of new vaccines. |
0 |
1 (5.3) |
0 |
12 (63.2) |
6 (31.6) |
|
1-5. It is necessary to form a working group to respond to a public health crisis or the spread of a specific infectious disease. |
0 |
0 |
2 (10.5) |
7 (36.8) |
10 (52.6) |
|
2. Submission of the agenda to KECIP |
|
|
|
|
|
|
2-1. An SOP for the submission of agenda items to KECIP should be prepared, and only relevant items should be submitted. |
0 |
5 (26.3) |
4 (21.1) |
9 (47.4) |
1 (5.3) |
|
2-2. Only agenda items judged by the KDCA to require the opinions of expert committee members should be submitted. |
0 |
9 (47.4) |
4 (21.1) |
5 (26.3) |
1 (5.3) |
|
2-3. If it is difficult for the KDCA to make its own judgment on whether to submit an agenda item, it should refer to the opinions of expert committee members and submit the agenda item. |
0 |
1 (5.3) |
0 |
13 (68.4) |
5 (26.3) |
|
3. Preparation of materials and time for agenda deliberation by members of KECIP |
|
|
|
|
|
|
3-1. The KDCA thoroughly reviews the agenda in advance and provides detailed deliberation materials to expert committee members. |
2 (10.5) |
2 (10.5) |
6 (31.6) |
8 (42.1) |
1 (5.3) |
|
3-2. The KDCA provides substantive meaning (up to behind-the-scenes studies) rather than providing only simple facts. Additionally, if it is difficult to express it in a document, it is explained over the phone in advance. |
1 (5.3) |
9 (47.4) |
7 (36.8) |
2 (10.5) |
0 |
|
3-3. The KDCA’s self-evaluation needs to be presented. |
0 |
3 (15.8) |
2 (10.5) |
9 (47.4) |
5 (26.3) |
|
3-4. If the data submitted by the vaccine manufacturer is insufficient, it is necessary to resubmit detailed data. |
0 |
1 (5.3) |
0 |
6 (31.6) |
12 (63.2) |
|
3-5. When requesting supplementation for incomplete documents or data, it is necessary to prepare related laws and regulations and background materials on similar matters. |
0 |
0 |
0 |
11 (57.9) |
8 (42.1) |
|
3-6. It is necessary to present fundamental problems that require expert deliberation. |
0 |
1 (5.3) |
0 |
9 (47.4) |
9 (47.4) |
|
3-7. There is insufficient clinical and epidemiological data to deliberate on the agenda. |
0 |
5 (26.3) |
6 (31.6) |
7 (36.8) |
1 (5.3) |
|
3-8. The meeting materials are distributed in advance so that expert committee members can sufficiently prepare for deliberation. |
2 (10.5) |
7 (36.8) |
7 (36.8) |
2 (10.5) |
1 (5.3) |
|
3-9. The current committee’s deliberation time is sufficient. |
2 (10.5) |
2 (10.5) |
7 (36.8) |
8 (42.1) |
0 |
|
3-10. It is necessary to adjust the size of the meeting, scope of attendance, and deliberation time according to the weight of the agenda rather than uniformly restricting the meeting. |
0 |
1 (5.3) |
0 |
11 (57.9) |
7 (36.8) |
|
3-11. The expert committee members should carefully review the data in advance and revise the questions to be discussed at the meeting or provide new questions. |
0 |
0 |
3 (15.8) |
10 (52.6) |
6 (31.6) |
|
3-12. The materials reviewed by expert committee members must be kept confidential, and if not, they may be held legally responsible. |
0 |
0 |
1 (5.3) |
12 (63.2) |
6 (31.6) |
|
4. Propose opinions from the perspective of vaccine manufacturers, citizens, and patients at KECIP meetings |
|
|
|
|
|
|
4-1. The opinions of vaccine manufacturers are sufficiently reflected in the meeting. |
0 |
4 (21.1) |
9 (47.4) |
6 (31.6) |
0 |
|
4-2. Vaccine manufacturers need to have the opportunity to accurately answer questions from expert committee members at KECIP meetings if deemed necessary. |
0 |
1 (5.3) |
3 (15.8) |
11 (57.9) |
4 (21.1) |
|
4-3. A written proposal is sufficient for the vaccine manufacturer's opinion. |
1 (5.3) |
8 (42.1) |
5 (26.3) |
5 (26.3) |
0 |
|
4-4. The public’s opinions are sufficiently reflected in KECIP meetings. |
1 (5.3) |
5 (26.3) |
6 (31.6) |
7 (36.8) |
0 |
|
4-5. The representatives of citizens/consumers should attend KECIP meetings and present their opinions. |
0 |
6 (31.6) |
2 (10.5) |
8 (42.1) |
3 (15.8) |
|
4-6. A written proposal is sufficient for public/consumer opinions. |
4 (21.1) |
8 (42.1) |
3 (15.8) |
4 (21.1) |
0 |
|
4-7. The position of consumers/patients can be sufficiently reflected by appointing members recommended by the public/consumer group as KECIP members. |
2 (10.5) |
7 (36.8) |
5 (26.3) |
5 (26.3) |
0 |
|
5. Impact of the decisions made by KECIP |
|
|
|
|
|
|
5-1. After the meeting, it is necessary to notify the members of KECIP whether the deliberation results were reflected in the final decision of the KDCA. |
0 |
0 |
1 (5.3) |
5 (26.3) |
13 (68.4) |
|
5-2. KECIP’s decision should, if possible, be reflected in the final decision stage of the KDCA. |
0 |
1 (5.3) |
2 (10.5) |
7 (36.8) |
9 (47.4) |
|
5-3. KECIP’s decisions should remain in the category of an advisory body. |
2 (10.5) |
6 (31.6) |
5 (26.3) |
4 (21.1) |
2 (10.5) |
|
6. Selection of expert committee members of KECIP |
|
|
|
|
|
|
6-1. The first criterion when selecting expert committee members is ‘expertise.’ |
0 |
0 |
0 |
7 (36.8) |
12 (63.2) |
|
6-2. When selecting expert committee members, it should be confirmed that there is no conflict of interest. |
0 |
1 (5.3) |
1 (5.3) |
4 (21.1) |
13 (68.4) |
|
6-3. When selecting expert committee members, members who have an interest in the relevant pharmaceutical company should be excluded from the deliberation meeting. |
0 |
2 (10.5) |
2 (10.5) |
5 (26.3) |
10 (52.6) |
|
6-4. The members selected as expert committee members should disclose their interests. |
0 |
0 |
1 (5.3) |
4 (21.1) |
14 (73.7) |
|
6-5. If it is deemed necessary for the efficient conduct of a meeting for an expert committee member with an interest in submitting an expert opinion in the relevant field, he/she attends the deliberation meeting but must be excluded from the decision-making process. |
0 |
0 |
3 (15.8) |
7 (36.8) |
9 (47.4) |
|
6-6. It is necessary to establish specific principles for selecting expert committee members. |
0 |
0 |
5 (26.3) |
7 (36.8) |
7 (36.8) |
|
7. Selection and role of the KECIP chairperson |
|
|
|
|
|
|
7-1. The chairperson should prepare in advance to ensure that the meeting proceeds efficiently by collecting professional opinions and revising the questions asked. |
0 |
0 |
1 (5.3) |
5 (26.3) |
13 (68.4) |
|
7-2. The chairperson can preside over the deliberation meeting and make decisions on whether the meeting will be public or private. |
0 |
0 |
2 (10.5) |
9 (47.4) |
8 (42.1) |
|
7-3. If deemed necessary, the chairperson could take all measures to ensure fair and prompt proceedings. |
0 |
0 |
1 (5.3) |
5 (26.3) |
13 (68.4) |
|
7-4. The chairperson should only perform the role of facilitator to ensure that the expert committee meetings proceed smoothly. |
3 (15.8) |
6 (31.6) |
4 (21.1) |
5 (26.3) |
1 (5.3) |
|
8. Role of expert committee members at KECIP meetings |
|
|
|
|
|
|
8-1. Expert committee members provide sufficient scientific and technical advice as experts in the relevant field regarding vaccination implementation and vaccines. |
0 |
0 |
1 (5.3) |
5 (26.3) |
13 (68.4) |
|
8-2. Expert committee members should play an advisory role regarding the enactment of relevant laws and regulations of the KDCA. |
0 |
1 (5.3) |
3 (15.8) |
8 (42.1) |
7 (36.8) |
|
8-3. Expert committee members should present fair and objective opinions on agenda items submitted to the meeting through expert discussions. |
0 |
0 |
1 (5.3) |
4 (21.1) |
14 (73.7) |
|
9. Disclosure of the results of the KECIP meeting |
|
|
|
|
|
|
9-1. There should be differences in disclosure methods depending on the agenda. |
0 |
1 (5.3) |
3 (15.8) |
10 (52.6) |
5 (26.3) |
|
9-2. Disclosure is not possible to submit confidential opinions. |
1 (5.3) |
10 (52.6) |
4 (21.1) |
2 (10.5) |
2 (10.5) |
|
9-3. The results should be made public to hold expert committee members accountable for their comments. |
1 (5.3) |
6 (31.6) |
6 (31.6) |
5 (26.3) |
1 (5.3) |
|
9-4. Expert committee meetings are, in principle, open to the public, but necessary parts (data presentation, committee deliberation) should be held privately. |
0 |
1 (5.3) |
3 (15.8) |
10 (52.6) |
5 (26.3) |
The multiple-choice questions used a 5-point scale, ranging from “strongly disagree” to “strongly agree.” For analysis purposes, the responses of “strongly disagree” and “disagree” were combined into “disagree,” while responses of “strongly agree” and “agree” were combined into “agree.” The survey results were tabulated using the number and percentage of respondents for each item’s scale. Excel (MS Office Excel 2018; Microsoft, Redmond, WI, USA) was used to construct the tables.
Ethics statement
This study was reviewed and approved by the Institutional Review Board (IRB) of Korea University Anam Hospital (IRB No. 224AN0067). Respondents were assured of anonymity and confidentiality, and web-based informed consent was obtained prior to the online survey.
RESULTS
A total of 19 experts participated in this survey, representing various fields of expertise: five in internal medicine (infectious diseases), four in pediatrics (infectious diseases), three in preventive medicine, one in pediatrics (other than infectious diseases), one in family medicine, one in public health epidemiology, one in statistics, one in microbiology, one in immunology, and one in a consumer group. The sex distribution was as follows: 14 male and five female. Regarding the experience in their fields, eight respondents had 26–30 years of experience, five respondents had more than 30 years, four respondents had 21–25 years, and two respondents had 16–20 years. In terms of experience within KECIP, 13 respondents had 1–5 years of experience, two respondents had 6–10 years, one respondent had 11–15 years, two respondents had 16–20 years, and one respondent had more than 30 years of experience. The responses to the 47 survey questions on the nine topics regarding the improvement of KECIP are represented in
Table 1.
Most respondents (73.7%) agreed with the current KECIP member count (15 people) and supported the maintenance of subcommittees (84.2%). Nearly all participants (94.7%) believed that the subcommittees should handle new vaccine agendas. Furthermore, the majority of respondents (89.5%) emphasized the need for establishing a dedicated crisis response team. However, opinions on the term length of KECIP were divided (36.8% disagreed, 42.1% agreed, and 21.1% were neutral). Opinions were divided on whether the KDCA thoroughly reviewed the agenda and provided detailed materials (47.4% agreed, 31.6% were neutral). Most participants felt that the KDCA’s self-evaluation was necessary (73.7%) and the majority of respondents (94.7%) indicated that incomplete data submitted by the vaccine manufacturer should prompt resubmission. The participants stressed the need for thorough preparation, including the background materials and laws (100% agreement). Adjusting the meeting size and time according to the agenda weight was favored (94.7%). Expert committee members were expected to review the data carefully (84.2%) and maintain confidentiality (94.7%). Moreover, there were concerns about insufficient clinical and epidemiological data for deliberation (42.1% agreed, 26.3% disagreed, and 31.6% were neutral). The distribution of meeting materials in advance was contentious (47.4% disagreed, 36.8% were neutral, and 15.8% agreed). Those seeking more preparation time suggest 1–2 weeks.
The opinions varied regarding the representation of vaccine manufacturers’ views, with most respondents being neutral (47.4%) and a few agreeing (31.6%). Additionally, there was a consensus (78.9%) that vaccine manufacturers should clarify queries at KECIP meetings. Regarding the public input, opinions were divided into a slightly higher percentage of agreement (36.8%) and remaining neutral (31.6%). Many believed that citizens/consumers should have the opportunity to participate in KECIP meetings (57.9%) and that a written proposal was not adequate for their input (63.1%). However, the respondents disagreed that a written proposal was sufficient for vaccine manufacturers’ opinions (47.4%). Regarding the consumer representation in KECIP, most disagreed (47.4%), with a few being neutral (26.3%), and a few agreed (26.3%).
The majority of respondents (94.7%) agreed that KECIP members should be notified of the KDCA’s final decisions after meetings. Several respondents (84.2%) believed that KECIP decisions should influence the KDCA’s final decisions. However, opinions vary on whether KECIP should remain solely advisory, with more disagreements (42.1%) than agreements (31.6%). All participants prioritized expertise as the primary criterion for the selection of expert members. Several participants (89.5%) emphasized the need to check for conflicts of interest, and 78.9% advocated the exclusion of members with ties to pharmaceutical companies. Most participants (94.7%) agreed to disclose their interests. While 84.2% of respondents permitted participation in relevant expertise, those with conflicts were excluded from decision-making. The establishment of specific selection principles was deemed necessary by 73.4% of respondents, including years of experience, verifiable research performance, and ethical considerations.
A vast majority of respondents (94.7%) believed that the chairperson should prepare in advance to streamline meetings, gather expert opinions, and refine questions. Additionally, 89.5% of respondents supported the chairperson’s authority to lead and make decisions regarding the meeting’s privacy. Similarly, 94.7% of respondents agreed that the chairperson could take the steps necessary for fair proceedings. However, opinions varied regarding whether the chairperson should simply facilitate, with 47.3% of respondents disagreeing, 31.6% of respondents agreeing, and 21.1% of respondents being neutral. Furthermore, most participants (94.7%) agreed that the expert committee members offered adequate scientific and technical advice on the implementation of immunization. Additionally, 78.9% believed they should advise on the KDCA’s laws and regulations. Similarly, 94.7% of participants supported the notion that expert committee members should provide fair and objective opinions during meetings. Regarding the disclosure methods, the majority of respondents (78.9%) suggested varying methods based on the agenda, and an equal proportion of respondents (78.9%) advocated public access to expert committee meetings, with certain parts being held privately. However, regarding confidentiality in disclosure, 57.9% of respondents disagreed with its necessity, 21.1% of respondents agreed, and 21.1% of respondents remained neutral. The opinions were evenly divided on making the results public for accountability: 36.8% disagreed, 31.6% were neutral, and 31.6% agreed.
DISCUSSION
Given the growing emphasis on the importance of preventing infectious diseases and the expanding goals and targets of immunization efforts, this survey provides a timely opportunity to reflect on the role of KECIP and its future directions. The National Immunization Technical Advisory Group serves as a crucial resource and decision-making body, providing evidence-based guidance to the national authorities amidst complex health systems and global interdependence.
4 During this survey, new challenges regarding the appropriate composition, role, qualification requirements, and selection methods of the committee were identified alongside KECIP’s existing functions of reviewing data, developing recommendations, and publishing updated national guidelines and immunization schedules.
5
Overall, most respondents supported maintaining the current member count and having subcommittees handle new vaccine agendas, while emphasizing the need for establishing workgroups. Opinions varied on the term length of KECIP and the thoroughness of agenda reviews by the KDCA. Most respondents stressed the importance of thorough preparation, careful data review, and maintaining confidentiality. There were concerns about insufficient clinical and epidemiological data, as well as varying opinions on public input and representation of vaccine manufacturers’ views. While most agreed that KECIP decisions should influence KDCA’s final decisions, opinions were split on whether KECIP should remain advisory. Criteria for expert member selection, the role of the chairperson, and disclosure methods were also discussed, highlighting the need for transparency and expertise in decision-making processes.
While KECIP has regulations that allow the establishment of a subcommittee, the current structure and functioning of this subcommittee are not well defined. In contrast, countries such as the United States,
6 the United Kingdom,
7 and Australia
8 use subcommittees or work groups to thoroughly examine specific topics and clarify issues, thus facilitating well-informed and efficient decision-making processes. The survey findings and discussions within the expert advisory subcommittee strongly emphasize the necessity for workgroups in South Korea. To enhance the efficiency of these workgroups, it could be beneficial to distinguish between permanent and non-permanent groups and regularly reassess their roles and research topics. Through the active participation of these workgroups, KECIP will be able to efficiently evaluate current vaccine usage and respond appropriately to the development and introduction of new vaccines.
The findings of this study underscore the critical role of KECIP in shaping national vaccination policies. With the increasing complexity of vaccine science and the emergence of new infectious diseases, there is a pressing need for robust and informed guidance from expert committees, such as KECIP. To fulfill this advanced role, KECIP should adopt a more inclusive approach to agenda setting, allowing for bottom-up suggestions and ensuring transparency in the decision-making process. Standard operating procedures should be developed to clarify the roles and operational methods of work groups. The committee should ensure that the experts participating are free from conflicts of interest, and it should explore avenues to incorporate diverse viewpoints while maintaining their expertise.
In conclusion, this study provides valuable insights into the current status and future directions of KECIP. Moving forward, efforts to strengthen KECIP’s capacity and effectiveness are essential for addressing evolving public health challenges and ensuring the continued success of vaccination programs in South Korea.