Apr 21, 2015 · Procedure for SOP Sign Off's? - posted in Documentation & Document Control: What are others procedures when it comes to approving SOPs and other documentation? Is it common to have approval signatures on each SOP? We do not have digital signatures, rather small company. If signatures are recommended, which personnel? We have Director or R&D, Product Compliance Manager, QC Manager and ...

Apr 9, 2013 · I disagree. I think signing each page is rooted deeply in the old ISO 9000 era when paper work for paper work sake was king. IMO it is necessary only to sign one page - the first page. This first page will also contain the control information such a unique document reference, number of pages in the document and the current issue of the document.

Mar 16, 2016 · SOP = Sanitize out of Place . The old "technical" line may have only required CIP, where that process would clean all necessary surfaces to an acceptable level. Your new "aseptic" line may require additional disassembly for COP and additional sanitizing (or the EU term, disinfection) to achieve the necessary cleanliness. Again, I'm making ...

Jul 15, 2021 · Each document also has the Revision, Revision Date, and SQF Practitioner Approval in the footers. When we both sign the document it goes into effect and the register of documents will be updated accordingly. I save the signed copy into a PDF and file it in our Quality Folder and I also keep a hard copy available in an SOP or Forms binder.

Aug 24, 2020 · All of this documentation (PPT training material, SOP, sign in sheet, final quiz with passing scores) must remain on file in the event you are audited by the FDA/Third Party/Customer, etc... and are required to prove that these employees have been properly trained.

May 21, 2014 · The SOP might be "QA-SOP-12.17.45A - SOP for button QC check"- 1. Push the red button with your left hand 2. Push the blue button with your right foot. 3. Push the green button with your left foot. 4.Push the purple button with your head 5. Push the orange button with your hip. 6. Record results on form 12.17.45B

Oct 22, 2012 · Training Program Requirements - posted in SQF Food: Hi all,Once again I am floundering around trying to understand the requirements of the SQF code and the expectations of the auditors - this time around training evaluation and competence sign off - and I was hoping someone here could help me out with some clarification.The code requirements for the training matrix/register states that: "A ...

Nov 1, 2021 · SOP for product trace SQF 2.6.2.1 - posted in SQF Food: Hello, I am looking for an example of SOP for product trace to fulfill item 2.6.2.1 of SQF 9. I have a recall plan in place and an SOP for mock recall exercises. Would it be sufficient? Thanks!

Nov 1, 2016 · From my experience: 1) need to have a SOP stating clearly do´s and dont´s; 2) verbally instruct the employees on the SOP; 3) in case of problem, give a formal instruction about the SOP, checking understanding; 4) persisting the problem, verbal advice; 5) still having problems, written advice from HR and then applying the appropriate measures.

Aug 6, 2020 · Our visitor and contract service provider SOP consists of a list of services we utilize and the requirements for each one (certs, licenses, required training, etc.) and also all of them are required to sign our visitor/contractor GMP policy acknowledging they understand the rules, which says stuff like tools cant be left out, work cant affect food safety, visitors must be …