Medical Waste Management Regulations to be Amendedwaste2000
「Medical Waste Management Regulations to be Amendedwaste2000」於資料集「Environmental Policy Monthly」由單位「行政院環境保護署」的楊先生所提供，聯繫電話是(02)23117722#2217,(02)23117722#2216，最近更新時間為：2022-01-15 01:13:03。 欄位編號的內容是383 ， 欄位標題的內容是Medical Waste Management Regulations to be Amended ， 欄位摘要的內容是The EPA recently held discussions on amending regulations concerning the storage clearance, and treatment of infectious medical waste. The draft amendment proposes loosening medical waste storage requirements. Moreover, the EPA will set different storage requirements according to storage site characteristics and functions. And, in order to maintain full knowledge of the destination of hazardous waste, the EPA will enforce regulations requiring medical institutions, waste clearance firms, and waste treatment firms to sign three-way agreements.
Domestic medical enterprises often comment that currently enacted medical waste management regulations are not suitable to all situations and are more stringent than those in other countries. Previously, in response to the suspension of operation order given to Jih-you, Taiwan’s largest medical waste disposal firm (over 50% of all medical wastes) for illegal waste handling, the EPA actively met with relevant firms to communicate and plan response measures. At this time it was discovered that current regulations governing the storage, clearance, and treatment of medical waste had some room for modification. The EPA therefore proposed amendments to the Standards for Industrial Waste Storage, Collection and Treatment Methods and Facilities and called together academics and experts and representatives from local-level environmental agencies, waste clearance firms, medical practitioner representatives to discuss the contents of the draft amendments.
The draft proposes loosening the time limitations on storing infectious medical waste. Articles have been added stipulating that infectious waste stored below zero degrees Celsius can be stored for up to 30 days.
However, local-level representatives have questioned this approach. They have requested the EPA to properly consider the ramifications on bacterial growth of low-temperature storage and freezing of infectious waste. They also requested the EPA to consider the ability of clearance firms to upgrade their transportation and storage equipment.
EPA Bureau of Solid Waste Management Director General, Shuh-Chiang Fu, stated that the EPA will fully consider the concerns raised. Director General Fu further revealed that the EPA is currently developing plans to separately establish storage criteria based on storage facility characteristics and functions. And future regulations may set different waste storage temperature and time criteria for medical institutions and clearance processes.
In addition, the EPA proposed replacing the practice of using different colored receptacles to distinguish wastes with a system which would directly separate medical wastes into two general categories: those which can and cannot be incinerated. These wastes would be separately collected and regulated. However this proposal met with opposition from industry members who expressed that the current system using red and yellow containers has been in effect for some time already and is easy to distinguish and manage. Any hasty decision to scrap it would be inappropriate. In light of this the EPA decided to adopt industry members opinions and continue use of the red and yellow containers.
Apart from items slated for amendment, EPA officials also expressed that in order to control the final storage site of hazardous waste in the future there will be compulsory regulations for three-sided agreements between medical establishments, collection firms and treatment organizations. Presently the majority of contracts signed between medical institutions and contracted collection and treatment firms are two-sided agreements. After a medical institution entrusts waste materials to a contracted collection institution for removal and transportation they assume they are absolved of all responsibility for the wastes. This has resulted in a number of difficult situations for the contracted firms and is equally difficult to supervise. For this reason the EPA is drafting strengthened legal regulations and in the future the subcontracting of industrial waste materials will require the industrial institution, the contracted collection firm and the contracted treatment institution to form a single body, singing a contract together and bearing joint responsibility.
In response to this decision by the EPA, attendees of the meeting suggested that the central government determine a model contract which would clearly normalize the rights and obligations of the three parties and provide specific channels for industry members to resolve future disputes.
During the meeting Chairman of the Chinese Doctors Association, Chao-Geng Lin, pointed out that for the infectious wastes produced every month by Chinese medicine institutions, such as the mere 100 to 200 needles used per week for acupuncture, according to current regulations not only is the cost of disposing of the wastes more expensive than the needles themselves, but the containers required at storage sites create more pollution than the wastes themselves. Mr. Lin suggested that the EPA formulate a set of reasonable practices for use by medical establishments that generate small amounts of waste, such as extending the time limit for storage in order to reduce the frequency of clearance and treatment.
In response to this the EPA expressed that if supporting measures could be improved they would not rule out considerations of extending the time limits for storage. Another possibility would be to draw up a plan similar to the joint water processing systems used by small-scale factories. Medical institutions within a given area could collectively sign a contract with clearance and treatment firms to jointly undertake related environmental responsibilities. However, this method is not in accordance with current inspection regulations so it would be necessary to revise these regulations.
Furthermore, scholars in attendance once again called for the loosening of regulations for long disputed medical waste items such as wooden tongue depressors and blood stained cotton balls by classifying them as common waste materials. The scholars expressed that according to scientific principle, by treating them with a high temperature sanitation process, these materials can be rendered harmless to the environment and common burial or incineration practices can be used for their disposal.
The EPA believes though that the sanitation disposal equipment currently used at most domestic county and city burial sites are not yet perfect, furthermore total implementation of the use of incinerators will not be completed until 2003. In order to ensure the safety of public sanitation, in principle the EPA leans towards classifying the disputed materials as infectious waste for treatment purposes and it is unlikely that there will be future revisions to this policy. ， 欄位全文的內容是The EPA recently held discussions on amending regulations concerning the storage clearance, and treatment of infectious medical waste. The draft amendment proposes loosening medical waste storage requirements. Moreover, the EPA will set different storage requirements according to storage site characteristics and functions. And, in order to maintain full knowledge of the destination of hazardous waste, the EPA will enforce regulations requiring medical institutions, waste clearance firms, and waste treatment firms to sign three-way agreements.
Domestic medical enterprises often comment that currently enacted medical waste management regulations are not suitable to all situations and are more stringent than those in other countries. Previously, in response to the suspension of operation order given to Jih-you, Taiwan’s largest medical waste disposal firm (over 50% of all medical wastes) for illegal waste handling, the EPA actively met with relevant firms to communicate and plan response measures. At this time it was discovered that current regulations governing the storage, clearance, and treatment of medical waste had some room for modification. The EPA therefore proposed amendments to the Standards for Industrial Waste Storage, Collection and Treatment Methods and Facilities and called together academics and experts and representatives from local-level environmental agencies, waste clearance firms, medical practitioner representatives to discuss the contents of the draft amendments.
The draft proposes loosening the time limitations on storing infectious medical waste. Articles have been added stipulating that infectious waste stored below zero degrees Celsius can be stored for up to 30 days.
However, local-level representatives have questioned this approach. They have requested the EPA to properly consider the ramifications on bacterial growth of low-temperature storage and freezing of infectious waste. They also requested the EPA to consider the ability of clearance firms to upgrade their transportation and storage equipment.
EPA Bureau of Solid Waste Management Director General, Shuh-Chiang Fu, stated that the EPA will fully consider the concerns raised. Director General Fu further revealed that the EPA is currently developing plans to separately establish storage criteria based on storage facility characteristics and functions. And future regulations may set different waste storage temperature and time criteria for medical institutions and clearance processes.
In addition, the EPA proposed replacing the practice of using different colored receptacles to distinguish wastes with a system which would directly separate medical wastes into two general categories: those which can and cannot be incinerated. These wastes would be separately collected and regulated. However this proposal met with opposition from industry members who expressed that the current system using red and yellow containers has been in effect for some time already and is easy to distinguish and manage. Any hasty decision to scrap it would be inappropriate. In light of this the EPA decided to adopt industry members opinions and continue use of the red and yellow containers.
Apart from items slated for amendment, EPA officials also expressed that in order to control the final storage site of hazardous waste in the future there will be compulsory regulations for three-sided agreements between medical establishments, collection firms and treatment organizations. Presently the majority of contracts signed between medical institutions and contracted collection and treatment firms are two-sided agreements. After a medical institution entrusts waste materials to a contracted collection institution for removal and transportation they assume they are absolved of all responsibility for the wastes. This has resulted in a number of difficult situations for the contracted firms and is equally difficult to supervise. For this reason the EPA is drafting strengthened legal regulations and in the future the subcontracting of industrial waste materials will require the industrial institution, the contracted collection firm and the contracted treatment institution to form a single body, singing a contract together and bearing joint responsibility.
In response to this decision by the EPA, attendees of the meeting suggested that the central government determine a model contract which would clearly normalize the rights and obligations of the three parties and provide specific channels for industry members to resolve future disputes.
During the meeting Chairman of the Chinese Doctors Association, Chao-Geng Lin, pointed out that for the infectious wastes produced every month by Chinese medicine institutions, such as the mere 100 to 200 needles used per week for acupuncture, according to current regulations not only is the cost of disposing of the wastes more expensive than the needles themselves, but the containers required at storage sites create more pollution than the wastes themselves. Mr. Lin suggested that the EPA formulate a set of reasonable practices for use by medical establishments that generate small amounts of waste, such as extending the time limit for storage in order to reduce the frequency of clearance and treatment.
In response to this the EPA expressed that if supporting measures could be improved they would not rule out considerations of extending the time limits for storage. Another possibility would be to draw up a plan similar to the joint water processing systems used by small-scale factories. Medical institutions within a given area could collectively sign a contract with clearance and treatment firms to jointly undertake related environmental responsibilities. However, this method is not in accordance with current inspection regulations so it would be necessary to revise these regulations.
Furthermore, scholars in attendance once again called for the loosening of regulations for long disputed medical waste items such as wooden tongue depressors and blood stained cotton balls by classifying them as common waste materials. The scholars expressed that according to scientific principle, by treating them with a high temperature sanitation process, these materials can be rendered harmless to the environment and common burial or incineration practices can be used for their disposal.
The EPA believes though that the sanitation disposal equipment currently used at most domestic county and city burial sites are not yet perfect, furthermore total implementation of the use of incinerators will not be completed until 2003. In order to ensure the safety of public sanitation, in principle the EPA leans towards classifying the disputed materials as infectious waste for treatment purposes and it is unlikely that there will be future revisions to this policy. ， 欄位年度的內容是2000 ， 欄位月份的內容是3 ， 欄位卷的內容是3 ， 欄位期的內容是1 ， 欄位順序的內容是1 ， 欄位倒序的內容是2 ， 欄位分類的內容是waste ， 欄位標題2的內容是Medical Waste Management Regulations to be Amended ， 欄位檔案位置的內容是print/V3/V3-01 。
編號
383
標題
Medical Waste Management Regulations to be Amended
摘要
The EPA recently held discussions on amending regulations concerning the storage clearance, and treatment of infectious medical waste. The draft amendment proposes loosening medical waste storage requirements. Moreover, the EPA will set different storage requirements according to storage site characteristics and functions. And, in order to maintain full knowledge of the destination of hazardous waste, the EPA will enforce regulations requiring medical institutions, waste clearance firms, and waste treatment firms to sign three-way agreements. Domestic medical enterprises often comment that currently enacted medical waste management regulations are not suitable to all situations and are more stringent than those in other countries. Previously, in response to the suspension of operation order given to Jih-you, Taiwan’s largest medical waste disposal firm (over 50% of all medical wastes) for illegal waste handling, the EPA actively met with relevant firms to communicate and plan response measures. At this time it was discovered that current regulations governing the storage, clearance, and treatment of medical waste had some room for modification. The EPA therefore proposed amendments to the Standards for Industrial Waste Storage, Collection and Treatment Methods and Facilities and called together academics and experts and representatives from local-level environmental agencies, waste clearance firms, medical practitioner representatives to discuss the contents of the draft amendments. The draft proposes loosening the time limitations on storing infectious medical waste. Articles have been added stipulating that infectious waste stored below zero degrees Celsius can be stored for up to 30 days. However, local-level representatives have questioned this approach. They have requested the EPA to properly consider the ramifications on bacterial growth of low-temperature storage and freezing of infectious waste. They also requested the EPA to consider the ability of clearance firms to upgrade their transportation and storage equipment. EPA Bureau of Solid Waste Management Director General, Shuh-Chiang Fu, stated that the EPA will fully consider the concerns raised. Director General Fu further revealed that the EPA is currently developing plans to separately establish storage criteria based on storage facility characteristics and functions. And future regulations may set different waste storage temperature and time criteria for medical institutions and clearance processes. In addition, the EPA proposed replacing the practice of using different colored receptacles to distinguish wastes with a system which would directly separate medical wastes into two general categories: those which can and cannot be incinerated. These wastes would be separately collected and regulated. However this proposal met with opposition from industry members who expressed that the current system using red and yellow containers has been in effect for some time already and is easy to distinguish and manage. Any hasty decision to scrap it would be inappropriate. In light of this the EPA decided to adopt industry members opinions and continue use of the red and yellow containers. Apart from items slated for amendment, EPA officials also expressed that in order to control the final storage site of hazardous waste in the future there will be compulsory regulations for three-sided agreements between medical establishments, collection firms and treatment organizations. Presently the majority of contracts signed between medical institutions and contracted collection and treatment firms are two-sided agreements. After a medical institution entrusts waste materials to a contracted collection institution for removal and transportation they assume they are absolved of all responsibility for the wastes. This has resulted in a number of difficult situations for the contracted firms and is equally difficult to supervise. For this reason the EPA is drafting strengthened legal regulations and in the future the subcontracting of industrial waste materials will require the industrial institution, the contracted collection firm and the contracted treatment institution to form a single body, singing a contract together and bearing joint responsibility. In response to this decision by the EPA, attendees of the meeting suggested that the central government determine a model contract which would clearly normalize the rights and obligations of the three parties and provide specific channels for industry members to resolve future disputes. During the meeting Chairman of the Chinese Doctors Association, Chao-Geng Lin, pointed out that for the infectious wastes produced every month by Chinese medicine institutions, such as the mere 100 to 200 needles used per week for acupuncture, according to current regulations not only is the cost of disposing of the wastes more expensive than the needles themselves, but the containers required at storage sites create more pollution than the wastes themselves. Mr. Lin suggested that the EPA formulate a set of reasonable practices for use by medical establishments that generate small amounts of waste, such as extending the time limit for storage in order to reduce the frequency of clearance and treatment. In response to this the EPA expressed that if supporting measures could be improved they would not rule out considerations of extending the time limits for storage. Another possibility would be to draw up a plan similar to the joint water processing systems used by small-scale factories. Medical institutions within a given area could collectively sign a contract with clearance and treatment firms to jointly undertake related environmental responsibilities. However, this method is not in accordance with current inspection regulations so it would be necessary to revise these regulations. Furthermore, scholars in attendance once again called for the loosening of regulations for long disputed medical waste items such as wooden tongue depressors and blood stained cotton balls by classifying them as common waste materials. The scholars expressed that according to scientific principle, by treating them with a high temperature sanitation process, these materials can be rendered harmless to the environment and common burial or incineration practices can be used for their disposal. The EPA believes though that the sanitation disposal equipment currently used at most domestic county and city burial sites are not yet perfect, furthermore total implementation of the use of incinerators will not be completed until 2003. In order to ensure the safety of public sanitation, in principle the EPA leans towards classifying the disputed materials as infectious waste for treatment purposes and it is unlikely that there will be future revisions to this policy.
全文
The EPA recently held discussions on amending regulations concerning the storage clearance, and treatment of infectious medical waste. The draft amendment proposes loosening medical waste storage requirements. Moreover, the EPA will set different storage requirements according to storage site characteristics and functions. And, in order to maintain full knowledge of the destination of hazardous waste, the EPA will enforce regulations requiring medical institutions, waste clearance firms, and waste treatment firms to sign three-way agreements. Domestic medical enterprises often comment that currently enacted medical waste management regulations are not suitable to all situations and are more stringent than those in other countries. Previously, in response to the suspension of operation order given to Jih-you, Taiwan’s largest medical waste disposal firm (over 50% of all medical wastes) for illegal waste handling, the EPA actively met with relevant firms to communicate and plan response measures. At this time it was discovered that current regulations governing the storage, clearance, and treatment of medical waste had some room for modification. The EPA therefore proposed amendments to the Standards for Industrial Waste Storage, Collection and Treatment Methods and Facilities and called together academics and experts and representatives from local-level environmental agencies, waste clearance firms, medical practitioner representatives to discuss the contents of the draft amendments. The draft proposes loosening the time limitations on storing infectious medical waste. Articles have been added stipulating that infectious waste stored below zero degrees Celsius can be stored for up to 30 days. However, local-level representatives have questioned this approach. They have requested the EPA to properly consider the ramifications on bacterial growth of low-temperature storage and freezing of infectious waste. They also requested the EPA to consider the ability of clearance firms to upgrade their transportation and storage equipment. EPA Bureau of Solid Waste Management Director General, Shuh-Chiang Fu, stated that the EPA will fully consider the concerns raised. Director General Fu further revealed that the EPA is currently developing plans to separately establish storage criteria based on storage facility characteristics and functions. And future regulations may set different waste storage temperature and time criteria for medical institutions and clearance processes. In addition, the EPA proposed replacing the practice of using different colored receptacles to distinguish wastes with a system which would directly separate medical wastes into two general categories: those which can and cannot be incinerated. These wastes would be separately collected and regulated. However this proposal met with opposition from industry members who expressed that the current system using red and yellow containers has been in effect for some time already and is easy to distinguish and manage. Any hasty decision to scrap it would be inappropriate. In light of this the EPA decided to adopt industry members opinions and continue use of the red and yellow containers. Apart from items slated for amendment, EPA officials also expressed that in order to control the final storage site of hazardous waste in the future there will be compulsory regulations for three-sided agreements between medical establishments, collection firms and treatment organizations. Presently the majority of contracts signed between medical institutions and contracted collection and treatment firms are two-sided agreements. After a medical institution entrusts waste materials to a contracted collection institution for removal and transportation they assume they are absolved of all responsibility for the wastes. This has resulted in a number of difficult situations for the contracted firms and is equally difficult to supervise. For this reason the EPA is drafting strengthened legal regulations and in the future the subcontracting of industrial waste materials will require the industrial institution, the contracted collection firm and the contracted treatment institution to form a single body, singing a contract together and bearing joint responsibility. In response to this decision by the EPA, attendees of the meeting suggested that the central government determine a model contract which would clearly normalize the rights and obligations of the three parties and provide specific channels for industry members to resolve future disputes. During the meeting Chairman of the Chinese Doctors Association, Chao-Geng Lin, pointed out that for the infectious wastes produced every month by Chinese medicine institutions, such as the mere 100 to 200 needles used per week for acupuncture, according to current regulations not only is the cost of disposing of the wastes more expensive than the needles themselves, but the containers required at storage sites create more pollution than the wastes themselves. Mr. Lin suggested that the EPA formulate a set of reasonable practices for use by medical establishments that generate small amounts of waste, such as extending the time limit for storage in order to reduce the frequency of clearance and treatment. In response to this the EPA expressed that if supporting measures could be improved they would not rule out considerations of extending the time limits for storage. Another possibility would be to draw up a plan similar to the joint water processing systems used by small-scale factories. Medical institutions within a given area could collectively sign a contract with clearance and treatment firms to jointly undertake related environmental responsibilities. However, this method is not in accordance with current inspection regulations so it would be necessary to revise these regulations. Furthermore, scholars in attendance once again called for the loosening of regulations for long disputed medical waste items such as wooden tongue depressors and blood stained cotton balls by classifying them as common waste materials. The scholars expressed that according to scientific principle, by treating them with a high temperature sanitation process, these materials can be rendered harmless to the environment and common burial or incineration practices can be used for their disposal. The EPA believes though that the sanitation disposal equipment currently used at most domestic county and city burial sites are not yet perfect, furthermore total implementation of the use of incinerators will not be completed until 2003. In order to ensure the safety of public sanitation, in principle the EPA leans towards classifying the disputed materials as infectious waste for treatment purposes and it is unlikely that there will be future revisions to this policy.
年度
2000
月份
3
卷
3
期
1
順序
1
倒序
2
分類
waste
標題2
Medical Waste Management Regulations to be Amended
檔案位置
print/V3/V3-01
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不定期更新更新,47蔡先生 | 02-23257399#55723 | 2023-08-09 01:04:24
行政院環境保護署全國一般廢棄物產生量
每1月更新,92顏先生 | 02-23117722#2109 | 2023-07-27 01:01:24
行政院環境保護署歷年環保署農地營運中含鉛製程事業之土壤污染潛勢調查
不定期更新更新,52詹小姐 | 02-23117722 #8204 | 2022-01-14 01:20:28
行政院環境保護署應回收廢棄物稽核認證行程
每1年更新,117廖小姐 | 02-2370-5888#3103 | 2023-07-27 01:00:00
行政院環境保護署空氣品質小時值_南投縣_埔里站
每1時更新,142陳先生 | 02-2311-7722#2386 | 2023-08-02 00:57:26
行政院環境保護署
環保標章產品審查通過及有效數資料(第二類)
每1月更新,41盧小姐 | 02-23117722#2943 | 2023-07-27 01:03:55
行政院環境保護署空氣品質小時值_嘉義市_嘉義站
每1時更新,104陳先生 | 02-2311-7722#2386 | 2023-08-02 00:57:48
行政院環境保護署空氣品質小時值_新北市_新店站
每1時更新,153陳先生 | 02-2311-7722#2386 | 2023-08-02 00:58:21
行政院環境保護署空氣污染實收罰鍰
每年更新更新,122謝小姐 | 02-23117722#2103 | 2022-01-14 01:22:40
行政院環境保護署廢家具修繕DIY
不定期更新更新,41林小姐 | 04-22521718#53511 | 2023-08-09 01:04:04
行政院環境保護署
焚化爐煙囪位置圖
不定期更新更新,54張小姐 | 02-23712121#5907 | 2023-07-27 01:06:06
行政院環境保護署MajorEnvironmentalPolicies
每3月更新,163陳小姐 | (02)23117722#2753,(02)23117722#2756 | 2023-07-30 01:03:45
行政院環境保護署底泥申報各類水體數量
不定期更新更新,47張小姐 | 02-2383-2389 #8401 | 2022-01-14 01:20:30
行政院環境保護署雲林縣水量水質自動監測連線傳輸監測紀錄值即時資料集
不定期更新更新,47許先生 | 02-2311-7722#2831 | 2022-01-18 01:24:47
行政院環境保護署執行機關一般廢棄物處理量
每1月更新,167顏先生 | 02-23117722#2109 | 2023-07-27 01:01:19
行政院環境保護署
新竹市重要環保統計資料
每1月更新,164顏先生 | 02-23117722#2109 | 2023-08-07 00:59:59
行政院環境保護署核能四廠環境監測資料
不定期更新更新,34陳先生 | 04-22521718#51207 | 2022-01-14 01:22:00
行政院環境保護署環保標章驗證機構資料
每1月更新,40盧小姐 | 02-23117722#2943 | 2023-07-28 11:36:20
行政院環境保護署環保專案摘要資料_噪音振動
不定期更新更新,91陳先生 | 02-2311-7722#2386 | 2023-07-30 01:02:05
行政院環境保護署0800資源回收免費專線-整體話務達成狀況統計
每年更新更新,44莊先生 | 02-23705888#3108 | 2022-01-14 01:24:32
行政院環境保護署
Environmental Policy Monthly
不更新更新,178楊先生 | (02)23117722#2217,(02)23117722#2216 | 2022-01-15 01:13:03
行政院環境保護署管制事業下水道系統環工技師專責人員證號資料資訊平台
不定期更新更新,57葉先生 | 02-2311-7722#2821 | 2023-08-09 01:05:18
行政院環境保護署空氣品質小時值_新北市_土城站
每1時更新,208陳先生 | 02-2311-7722#2386 | 2023-08-02 00:58:19
行政院環境保護署環境用藥製造業地理資料
不定期更新更新,43王小姐 | 02-2325-7399#55413 | 2022-01-15 01:10:37
行政院環境保護署水污染管制區範圍地理圖資
不定期更新更新,59陳先生 | 02-23117722#2818 | 2023-08-07 01:04:26
行政院環境保護署