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Procedure for blocking and release of all materials


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#1 MOURADTALBI

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Posted 04 June 2019 - 07:43 AM

hi,

 

A procedure must be in place for the blocking and release of all raw materials, semi-finished and finished products and packaging materials.



#2 SQFconsultant

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Posted 04 June 2019 - 01:29 PM

Ah, is this a statement or request for something?


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#3 MOURADTALBI

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Posted 04 June 2019 - 04:24 PM

Ah, is this a statement or request for something?

it's a requirement for IFS food and I'm looking for a documented procedure to meet this requirement
 
I'm sorry for my missing request


#4 Sandima

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Posted 05 June 2019 - 06:18 PM

We use a computerized inventory system so items are received/manufactured in a status that blocks the use/shipping of them until they have been approved and the status updated.



#5 Hank Major

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Posted 05 June 2019 - 08:43 PM

Here is some material to help you: an SOP, a Hold and Release Plan, and a Hold Placard.

 

 

 

Attached Files



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#6 Qualified

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Posted 06 June 2019 - 01:00 AM

 

it's a requirement for IFS food and I'm looking for a documented procedure to meet this requirement
 
I'm sorry for my missing request

 

something to work from

 

http://www.mascotpec...ing-product.pdf



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#7 MOURADTALBI

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Posted 06 June 2019 - 08:13 AM

Here is some material to help you: an SOP, a Hold and Release Plan, and a Hold Placard.

Thank you  for   sharing



#8 Charles.C

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Posted 06 June 2019 - 01:47 PM

Here is some material to help you: an SOP, a Hold and Release Plan, and a Hold Placard.

 

Hi Hank,

 

Thanks for useful example however I found it slightly odd in that there seems no specific mention of  -

 

(a) lack of compliance to a specification (eg BRC 3.8),

(b) Positive/Negative Release (eg BRC 5.7.1)

(c) non-conforming product having a scope wider than representing a "threat" to public health (eg BRC Glossary).

 

Regardless, appreciate the SOP.


Kind Regards,

 

Charles.C


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#9 Hank Major

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Posted 07 June 2019 - 07:49 PM

Hi Hank,

 

Thanks for useful example however I found it slightly odd in that there seems no specific mention of  -

 

(a) lack of compliance to a specification (eg BRC 3.8),

(b) Positive/Negative Release (eg BRC 5.7.1)

(c) non-conforming product having a scope wider than representing a "threat" to public health (eg BRC Glossary).

 

Regardless, appreciate the SOP.

 

Criticisms are good.  I already felt that the material was a little weak, which is why I said it was "some material to help" the OP.  I'll take a look at the BRC Clauses and Glossary you mentioned and probably revise my stuff.  Thanks.






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