SBS - The best value in QMS software

Hazard Analysis and Critical Control Points (HACCP) for Water?

N

noorsuhaida

#11
i'm so excited to knowing that u involved in ISO standard so long.actually i'm not food science student. suddenly i get involved in food industry after taken a short course under SIRIM. i'm happy to share about food industry better with you. Auditor from SIRIM that suggest my management not to go for ISO 22000. only go for HACCP certificate. but i said to them,ISO 22000 more convenience and more useful for food safety because it more details. we already have ISO 9001 .my management will decide it after re-assessment audit by early august. Thanks a lot for your advice. for reverse osmosis,can u advice me where is CCP in our process. i attached my process in this reply

:D
 

Attachments

Elsmar Forum Sponsor
S

Soon Loy

#12
You had done a good job for a lady who was not trained in this field but under ISO 22000 you would need to do a little bit more (not much more though). IMO from what was given in the process flow, your CCPs would be at the a) filtering by RO Membrane as the final step for removing potential foreign agents; b) microbial removal / reduction by UV Lighting. All others are presumably controlled by verification and / or supported by validation activities.

Why do you want to name a specific bactericidal i.e. "Diversol CX" - if you change bactericidal agent w/o a review or approval for change, this will automatically become a "NC" (wise to leave it as "bactericidal agent)

BTW, I am not aware of SIRIM being accredited to any Accreditation Body for the issuance of accredited certification for ISO 22000:2005.
 
N

noorsuhaida

#13
as i know,SIRIM is a certified body to give certification in Malaysia. but it is enjoyable audited by auditor from SIRIM rather than auditor from others. because auditor from SIRIM is strict,so we can know more about the auditing and the problem that need to solve. Diversol CX is a chlorine powder that act as disinfectant agent when our production worker wash outer and inner part of bottle. can i know,to kill microorganism what is the best temperature of hot water? because my colleague always argue the temperature of water with auditor. auditor said the temperature of hot water must 100 degree celcius. it is true?
 
S

Soon Loy

#14
Depending on which microbial strains you wish to destroy. From a hazard risk assessment point of view, you will need to know your targeted pathogens for your product in order to ensure safe quality integrity can be consistently delivered. Otherwise, it is impossible to establish the appropriate "kill step" with the appropriate means or method including the dosage intensity of your chlorine.

(Microbial strains differ from products to products) including protozoa in this instance.
 
N

noorsuhaida

#15
i don't know but maybe mesophilic microbe. for drinking water,the microbe that involved is E.Coli, faecal coliform and total coliform. where i can get the information of microorganism?
 
S

Soon Loy

#16
Evidently, the disinfection process that you have taken is to eliminate microbes contaminated from mainly external sources i.e. customer's abuse or storage location; during transportation etc. Therefore, the microbes are pretty varied. My only other strong suggestion to you is to take a test for Pseudomonas Aeruginosa which is not a requirement under the Malaysian Food Act but its an important microbe to keep away from.
 

6thsense

Involved In Discussions
#18
I work for a company that makes Sugar containing beverages and also bottles Packaged Water. Our process starts at the Watertreatment plant where we treat water using a variety of chemicals including chlorine. For both the beverages and water the chlorine is removed but for the packaged water the chlorine free water is then run through an RO Unit. The water from the RO unit is then ozonated and packaged in PET bottles. No rapid test or monitoring is done for the Carbon filtration to remove chlorine, just tests for residual chlorine. The existing CCPs are Carbon Filtration and Ozonation. I have no problems with the Ozonation step but can Carbon filtration to remove Chlorine be considered a CCP?
 
E

everfresh

#19
ISO 22000 & HACCP Certification for Dairy Farms?

Hello,

I need documents details for ISO 22000 & HACCP certification means which documents are required to prepare for given above certification, e.g suppliers records etc
 
M

moha33

#20
Hello everyone;

am planing to obtain HACCP or ISO 22000 for Mineral water production. I am looking for good experienced consultant and microbiologist to help get done.
 
Thread starter Similar threads Forum Replies Date
F Medical Device HACCP (Hazard Analysis and Critical Control Point) Risk Management ISO 14971 - Medical Device Risk Management 2
K General HACCP (Hazard Analysis Critical Control Point) Questions Food Safety - ISO 22000, HACCP (21 CFR 120) 8
N Should it even be on the hazard analysis (software)? FMEA and Control Plans 2
A Risk-benefit Analysis - Hazard Analysis (HA) and FMEAs ISO 14971 - Medical Device Risk Management 18
S The Severity of a Medical Device Hazard - Risk Analysis Clarification ISO 14971 - Medical Device Risk Management 6
D Hazard analysis for our medical device - Hazards seem to overlap 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
D Biological and Chemical Risks to the user in the Hazard Analysis ISO 14971 - Medical Device Risk Management 1
R Risk Analysis and Hazard Identification concerning Clinical Decision Support Systems ISO 14971 - Medical Device Risk Management 1
S PMA Submission Software Hazard Analysis Document vs. Product Hazard Analysis doc ISO 14971 - Medical Device Risk Management 5
V FMEA vs. Process Hazard Analysis (PHA) FMEA and Control Plans 2
K When, whom, how to conduct hazard analysis of PRP?s, OPRP?s and CCP?s? Food Safety - ISO 22000, HACCP (21 CFR 120) 1
K Seeking guidance on Preliminary Steps to enable Hazard Analysis Food Safety - ISO 22000, HACCP (21 CFR 120) 1
W PHA (Preliminary Hazard Analysis) and Safety Case per UK MOD requirements Occupational Health & Safety Management Standards 2
W Medical Device FMEA vs. ISO 14971 to create our Hazard Analysis ISO 14971 - Medical Device Risk Management 2
A Correlating Hazard Analysis and DFMEA Risk Acceptability Criteria FMEA and Control Plans 8
W FMEA vs. Hazard Analysis per FDA interpretation 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 10
A Safety Hazard Analysis Report - Need format or an example AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
Ajit Basrur Risk Analysis using Fault Tree Analysis (FTA) or Hazard Operations Analysis (HAZOP) ISO 13485:2016 - Medical Device Quality Management Systems 6
L Risk Analysis Question - Estimating the likelihood of a hazard occuring ISO 13485:2016 - Medical Device Quality Management Systems 1
I Hazard Identification and Naming ISO 14971 - Medical Device Risk Management 10
C ISO 45001 6.1.2.1 Hazard Identification Occupational Health & Safety Management Standards 1
D Failure rate vs hazard rate vs rate of failure Reliability Analysis - Predictions, Testing and Standards 2
D Hazard symbols and labeling ISO 13485:2016 - Medical Device Quality Management Systems 1
T Assessing Hazard-Related Use Scenarios where control measures exist through standards IEC 62366 - Medical Device Usability Engineering 32
M Informational Work in progress at the FDA for biological evaluation – Color Hazard and RISk calculator (CHRIS) Medical Device and FDA Regulations and Standards News 0
A Fire hazard classification - Clause in IEC 60601 about gauze and electricity ISO 14971 - Medical Device Risk Management 0
S ISO 14971 Risk Management - Questions for Hazard identification ISO 14971 - Medical Device Risk Management 2
A Moving and positioning of patient - Mechanical hazard IEC 60601 - Medical Electrical Equipment Safety Standards Series 18
L No entanglement hazard of applied parts cables? IEC 60601 - Medical Electrical Equipment Safety Standards Series 4
E EN/UL/CSA 61010 -1 (ed3) Safety and use of Software to Prevent Electrical Hazard CE Marking (Conformité Européene) / CB Scheme 3
M Hazard Identification for Pest Control Activities Other ISO and International Standards and European Regulations 9
N Hazard Probability of Occurrence Definition ISO 14971 - Medical Device Risk Management 11
A ISO 14971 Figure E.1 that starts with Hazard and ends with Risk ISO 14971 - Medical Device Risk Management 3
M IVDD ER 8.3 Vs. Hazard Labelling Regulations - Which outranks? EU Medical Device Regulations 2
G Combining Aspect Impact and Hazard Risk Register Miscellaneous Environmental Standards and EMS Related Discussions 8
R Risks which must be Distinctly Identified - Harm, Hazard, Severity ISO 14971 - Medical Device Risk Management 7
S Hazard Identification and Risk Assessment - Can Risk Assessment be "Grandfathered"? Occupational Health & Safety Management Standards 4
2 Medical Device Hazard Risks - Normal Use Risks vs. Faulty Use Risks ISO 14971 - Medical Device Risk Management 4
K Regarding ISO 62304 Clause 7.3.3 - Hazard and Risk Controls IEC 62304 - Medical Device Software Life Cycle Processes 9
S Aspect vs. Impact and Hazard vs. Risk - Short/clear explanation & example Miscellaneous Environmental Standards and EMS Related Discussions 11
K Differences between "Hazard" and "Risk" in ISO 22000 Food Safety - ISO 22000, HACCP (21 CFR 120) 4
D Occupational Hazard....is it worth ? Imported Legacy Blogs 3
somashekar Lead acid Batteries inside DG set acoustic enclosure - What Hazard and Risk and how ? Occupational Health & Safety Management Standards 5
S Hazcom (Hazard Communication) Labels per GHS Requirements Miscellaneous Environmental Standards and EMS Related Discussions 6
S Applying HAZOP and FMEA methods for HSE Hazard Identification in Construction Occupational Health & Safety Management Standards 3
K Behaviour Assessment for Hazard Identification & Risk Assessment Occupational Health & Safety Management Standards 25
M Two situations where it is appropriate to add further Hazard Audits to Internal Audit Occupational Health & Safety Management Standards 8
S Why is the definition of Hazard (OHSAS) focused on Humans alone ? Occupational Health & Safety Management Standards 13
D HHE (Health Hazard Evaluations) vs. HRA (Health Risk Assessment) US Food and Drug Administration (FDA) 6
M Trace Hazard Mitigation Requirements to Code Qualification and Validation (including 21 CFR Part 11) 4

Similar threads

Top Bottom