How to initiate a QRM process

Traditionally Hazard analysis and critical control point (HACCP) was adopted to do the risk assessment, Recently quality risk assessment is followed that is more relevant to the pharmaceutical industries. The guideline on Quality risk assessment to protect patient in terms of quality safety and efficacy of medicines.

In QRM a systematic science based decision making with respect to risk shall be considered. To intiate the QRM the problem shall be identified including possible risk. Detailed information shall be gathered which can lead to potential hazard or have harmful effect on human health and is relevant for the risk assessment

Quality Risk Management

The pharmaceutical industries are considered to be the most critical industry as the substandard medicines may put the life of patients who are consuming these products at risk.  

There are different regulatory authority who keeps an eye on the pharmaceutical industries.. these regulatory authorities include not only Indian authorities but also authorities of those countries where the pharmaceutical manufacturers  are dispatching  there products.

Difference between Drug and medicine

Drug and Medicines are generally considered as identical though there is difference between the two terms.

Drug - is a substance that creates hallucination or a stimulant.

Medicine - is a substance which is taken for treatment of any disease. Medicine is also considered as science.

SOP on cleaning on hose pipe

Below is the standard operating procedure to clean the Hose pipes. In some manufacturing companies hose pipe is also known as flexible pipe.

How to plan a Self inspection or Internal Audit

Internal audits are important within the manufacturing facility to recheck the existing system and to give assurance that an organisation's internal controls are .operating effectively.

Six Brand of turmeric added to recall for excessive lead.

A New Jersey company has expanding its recall of ground turmeric nationwide. Excessive lead, which is particularly dangerous for pregnant women, infants and children has been confirmed in the spice.

For more information Visit website

http://www.foodsafetynews.com/2016/08/six-brands-of-tumeric-added-to-recall-for-excessive-lead/#.V6p8JPl961t

Procedure on Good Recording Practices

OBJECTIVE

To lay down a procedure for Good Recording Practices.

RESPONSIBILITY

Personnel - All departments.
Heads – All Departments

PROCEDURE

• Personnel shall make on line entries in the documents.
• The entries made by the operating personnel shall be checked and signed by the    supervising       personnel.
• No entry shall be over written.
• If anything is wrong do not over write it.

HOW TO DETERMINE QUALITY IMPACT ON THE PRODUCT

While determining the quality impact of any event identified in the manufacturing of an API, the below aspect shall be studied but not limited to

1. Does it affect the final application or use by the customer?
2. Does it affect the storage condition of the product?
3. Does it affect the packing of the product?
4. Does it affect the transportation of the product?
5. Does it affect the Human safety?
6. Does it affect the Critical control point?
7. Does it affect the stability of the product?

If yes to any of the above questionnaire than there is quality impact on the API product,
If No to all the above questionnaire than there is no quality impact on the API product.

In case there is a quality impact the disposition of the product is to be decided.

Readers may contact the author at anshuyadav.icgian@gmail.com.

Related Articles 

How to initiate QRM process

Quality Risk Management

AUTHOR: ANSHU YADAV

quallpharmaconsultancy@gmail.com

anshuyadav.icgian@gmail.com

US FDA announces approval for generic Glumetza

Sun Pharma  today announced that one of its subsidiaries has received final approval from US FDA for its Abbreviated New Drug Application (ANDA) for generic version of Glumetza, Metformin Hydrochloride extended release tablets 500 mg and 1000 mg.

These Metformin Hydrochloride extended release tablets are therapeutic equivalents of Santarus Inc.’s Glumetza 

For more information view website

http://www.indiainfoline.com/article/news-top-story/sun-pharma-announces-us-fda-approval-for-generic-glumetza-116080200340_1.html

DEVIATION CONTROL AND MANAGEMENT

The aim of the document is to contribute to the understanding of a quality risk management approach in the handling of deviations from practical perspective as per WHO expectations on the matter.

The document is in line with documents like ICH Q10 Pharmacuetical Quality System, ICH Q9 Quality Risk Management like WHO, FDA and EU requirement.

Procedure:

• Deviation: Any departure from an approved instruction or established standards [Glossary of ICH Q7 –Good manufacturing guide for active pharmaceutical ingredients]
• Event Categorisation
• Identification of an Event- Anything that happens or takes place, especially important for notification.
• The decision tree described in the Flow diagram Diagram  is a simplified risk assessment that answer the following questions when an event is encountered:
• Effect on the product attribute
• Effect on manufacturing operational parameter.
• Effect on the Product quality.
• Contradict or omit specified requirement.
• Effect on the cGMP
• The specified requirements mentioned in 1.2.2.4 may be from any of the following:
• Standard Operating procedures that may cover any subject.
• Inspection and testing protocols.
• Customer specified requirements.
• Regulatory requirement.
• Technical instruction.
• Specified parameters written in forms and formats, log books and registers.
• HACCP plan.
• Drawing
• Specifications
• Incidents
• If the answer is NO for questions 1.2.2.1 and 1.2.2.5 above, the event may be considered an Incident.
• On the contrary, if any of the answer for questions 1.2.2.1 and 1.2.2.5 is YES the event shall follow the path towards a deviation category.
• Deviation
• A deviation is a situation that has occurred either in a planned or unplanned manner. It may be on a product or a process.
• Planned Deviation: Any deviation from a documented procedure or specified requirement adopted deliberately as a temporary measures.
• Unplanned Deviation: Any deviation occurred in an unintentional manner due to system failure, equipment breakdown, human error or any unforeseen circumstances.
• Minor Deviation - When the deviation does not affect any quality attributes, an operational or manufacturing parameters, or an equipment or instrument associated with the process, it is considered as Minor deviation.
• Major Deviation- When the deviation affects the quality attributes, an operational or manufacturing parameters, or an equipment or instrument associated with the process, of which the impact to personnel/environment is unlikely, the deviation is categorise as Major deviation.
• Critical Deviation- When the deviation affects the quality attributes, an operational or manufacturing parameters, or an equipment or instrument associated with the process, of which the impact to personnel/environment is highly probable is categorise as critical deviation
• Event Handling
• Identification of an Event- Anything that happens or takes place, especially important for notification.
• Whenever such event comes to notice use format no. F01 (Mail to anshuyadav.icgian@gmail.com if format is required) to identify whether it is an incident or Deviation and to classify it as planned or unplanned deviation.
• If it is an unplanned deviation than use format No F02 (Mail to anshuyadav.icgian@gmail.com if format is required)  to classify it as minor, major or critical.
• If it is a planned deviation than use format No F03 (Change control format)
• If it is and minor deviation/ incident than use format No F04(Mail to anshuyadav.icgian@gmail.com if format is required)
• Steps to handing Minor Deviation/Incidentt:
• Description of an Event
• Correction
• Efficacy and Conclusion
• Recording
•  Monitoring

NOTE:

Minor deviation shall be reviewed by Manager QA, recommended by department HOD and approved by Head QA

• Handling major deviations/critical deviations
•  Description of an event
•  Correction
•  Efficacy and Conclusion
• Root cause investigation 
• Investigation shall be done by using  5 why technique etc.
• An investigation report shall be generated which shall have the below contents but not limited to :
• Reason for investigation(what event or finding prompted investigation, how and when happened)
• Describe what happened(when and where)
•  Identify other batches/lots affected
•  Identify root cause
• Quality Impact
• The Quality impact shall be assessed by Quality Risk Management SOP. If there is a quality impact the product is considered as non-confirming product.
• Recommendation from department head, approval from Head QA and authorization by Director TQM.
•  Validation impact/supporting document.
• Assessment of validation impact (Shall be done by Departmental Head/Head QA and Director TQM)
• CAPA
• Efficacy of corrective action
• Conclusion

  Note:      Major/Critical deviation shall be reviewed by Manager QA, recommended by department HOD and approved by Head QA and authorized by Director TQM.

•  Handling of planned deviation
• Description of an event
•  Justification for requirement of planned deviation
•  Quality Impact
• The Quality impact shall be assessed by Quality Risk Management SOP. If there is a quality impact the product is considered as non-confirming product 
•  Validation impact/supporting document.
•  Assessment of validation impact.
•  CAPA
•  Efficacy of corrective action
• Conclusion
• Recording
• Monitoring

Note:Planned deviation shall be reviewed by Manager QA, recommended by department HOD and approved by Head QA and authorised by Director TQM.

• QA shall retain the records irrespective of the approved / reject status of the deviation report and a photocopy of the same shall be filed with the subjected batch manufacturing / packing record/analytical reports.
• Wherever a deviation could affect multiple batches, e.g. due to equipment or facility failure or material or process deviation report, a photocopy of the same shall be filed with the subjected batch manufacturing / packing record / analytical report.
• If it is found that the deviation occurred on account of a faulty procedure or process, action shall be taken to amend the concerned document under company’s document change system for necessary amendments to the affected documents.
• QA personnel shall maintain the deviation log, department wise, and year wise as per the Deviation Control Log (Mail to anshuyadav.icgian@gmail.com).
• Deviation/INCIDENT control numbering system (For details mail to anshuyadav.icgian@gmail.com)

If there are any query, questions or suggestion related to the article, please mail back to anshuyadav.icgian@gmail.com.

AUTHOR: ANSHU YADAV

anshuyadav.icgian@gmail.com