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Các câu hỏi thường gặp (FAQ) về FEM 4.0
Chemicals

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How can we demonstrate compliance with Q11 and Q12 on RSL compliance? In addition to carrying out testing to "ensure there is a validation processes in place to ensure compliance", what other validation processes are acceptable?
In Q5, "Does your facility contribute to an analysis of lifecycle impacts for selecting alternative processes?", there is few tool to do this such as bluesign Xpert but it is not available. Can you share some best practice?
Is it mandatory to use ZDHC Gateway for checking the chemical inventory list for ZDHC MRSL?
Under the Chemicals Management section. What certification courses do responsible persons (Qualified Trainers) need to take?
Can a facility with multiple sub-factories located away from the main factory, extend the activities of their CMS team and apply all their CMS documents to the sub-factories on FEM self-assessment and verification?
We do not use chemicals in production. It seems we need to include MRSL conformance level in the chemicals inventory list, but our chemical suppliers don't register their chemicals on ZDHC platform, what can we input for the MRSL conformance level?
What should be included in the emergency chemical spill training for all employees?
The positive list in the How to Higg guidelines, does not clarify for non-production chemicals, where can we find this guidance?
Are textile manufacturers expected to do the toxicity assessment for chemicals instead of chemical manufacturers?
What should be done if the verifier found that there were chemicals in the in-check report that didn't match the facility's inventory during verification?

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How are chemical sub-storage areas defined?

05:08 Ngày 11 tháng 04 năm 2024
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FEM
FEM FAQ
FEM Chemicals

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