亚洲国产精品精华液网站_韩国公和熄三级在线观看_永久免费福利超清影视站_黄叶网男人的DV天堂_久久精品国产亚洲āV麻豆网站_欧美多人群p刺激交视频_黄片在线免费观看欧美_一级特黄AAA毛片_亚洲午夜中文日韩_欧美日韩一区电影在线观看

咨詢服務(wù) 培訓(xùn)服務(wù)
  肯達(dá)信服務(wù)熱線 CTS 統(tǒng)一客服電話
400-690-0031
 
 
首頁(yè)>咨詢服務(wù)>TESCO驗(yàn)廠咨詢
TESCO驗(yàn)廠咨詢--TESCO非食品標(biāo)準(zhǔn)(英文)(六)

Tesco Non Food Standard


1.7

Control Measures


Control measures must beassessed to determine whether they can prevent, eliminate or reduce the risk of all identified hazards to acceptable levels. Where there is no control measure, the product/process must be modified so a control measure can be applied.


1.7.1

Control Measures


The documentation shouldshow links to a specific prerequisite, rather than generic commenti.e.‘Pre-requisite’.

e.g Glass/Hard Plastic Control

1.8

Determination of CCPs


An effective justification system must be used to decide if controls areCCPs (Critical Control Points).


1.81

Determination of CCPs


A decision tree or equivalent must be used to determine if control measures are CCPs.

e.g. the Codex decision tree is used (Appendix 3)

1.9

Critical Limits

Critical limits must be defined and validated where relevantto ensure that the product is safe. The process must be capable of operating consistently within the definedlimits. Critical limits must be measurable.

Critical limits are justified and documented.

The precision limits andtolerances of the monitoring equipment must be considered when defining limits.

1.10

Monitoring

Procedures &

Records


Documented CCP monitoring procedures must be established with clearlydefined frequencies to determine if the criticallimits are achieved. Records mustbe signedby the person doing the monitoring.

When identified by risk assessment records may need to be verified by

an authorised individual.


1.11

Corrective

Actions


When a CCP deviates fromcritical limits the corrective action required must be documented.The corrective actions must identify and isolateall defective materials and ensure that the CCP returns to operating within the critical limits.

If the safety of the product is in doubt, product or materials must be disposed of.


1.12

Verification

The HACCP/Risk Assessment planmust be verified to confirm that it is effective.

Verification may include:Internal audits

? Review of customer complaints

? Review of monitoring results

1.13

HACCP/ Risk

Assessment

Review


The HACCP plan / Risk Assessment must be reviewed either annually as a minimum, or prior to any changes of the product formulation or process which may affect product safety or legality.

Review following changesto:

1.Process steps

2.Raw material specifications

3.Formulation

4.Packaging, storage or distribution



客服中心
楊老師
王老師
徐老師
郭小姐
張小姐
陳老師
您好,我是肯達(dá)信管理顧問(wèn)公司客服,歡迎咨詢!

楊老師

您好,我是肯達(dá)信管理顧問(wèn)公司客服,歡迎咨詢!

王老師

您好,我是肯達(dá)信管理顧問(wèn)公司客服,歡迎咨詢!

徐老師

您好,我是肯達(dá)信管理顧問(wèn)公司客服,歡迎咨詢!

郭小姐

您好,我是肯達(dá)信管理顧問(wèn)公司客服,歡迎咨詢!

張小姐

您好,我是肯達(dá)信管理顧問(wèn)公司客服,歡迎咨詢!

陳小姐


客戶服務(wù)熱線

400-690-0031

24小時(shí)熱線

18576401396


展開(kāi)客服