004 Define Flashcards

1
Q

Define Validation

A

Validation in HACCP ensures the food safety plan effectively controls hazards. It confirms the measures in place achieve the desired safety outcomes.

  • Validation ensures that processes or systems consistently produce desired outcomes.

Validation is critical in HACCP, where ensuring the effectiveness of manufacturing processes is essential for product quality and safety.

Validation processes typically involve experimental studies and documentation to demonstrate that the process consistently meets predetermined specifications and quality attributes.

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2
Q

Define Accreditation

A

Formal recognition that a body or person is competent to perform specific tasks.

  • Accreditation ensures credibility and reliability in conformity assessment activities.

Accreditation is often granted by recognized accreditation bodies after a rigorous evaluation of competence, impartiality, and consistency.

Accreditation enhances confidence in the competence and reliability of conformity assessment bodies, supporting international trade and market access.

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3
Q

Define Continual Improvement

A

Ongoing process of enhancing products, services, or processes to achieve better performance, efficiency, and effectiveness.

  • Continual improvement is a key principle in quality management systems.

Continual improvement involves regular reviews, adjustments, and innovations to enhance organizational performance and meet changing customer needs.

Implementing continual improvement fosters a culture of innovation, efficiency, and customer satisfaction within organizations.

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4
Q

Define Traceability

A

The ability to trace the history, application, or location of an item or activity by means of recorded identification.

  • Traceability ensures transparency and accountability in supply chains and production processes.

Traceability is crucial in food safety and quality management to quickly identify and address issues such as product recalls or quality deviations.

Traceability systems use unique identifiers, labeling, and documentation to track product movements and ensure compliance with regulatory requirements.

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5
Q

Define Critical Limit

A

The maximum or minimum value to which a biological, chemical, or physical parameter must be controlled at a Critical Control Point (CCP) to prevent, eliminate, or reduce a hazard to an acceptable level.

  • Critical limits are established in HACCP systems to ensure food safety.

Critical limits are determined based on scientific data and risk assessment to effectively control identified hazards in food production processes.

Monitoring critical limits is essential for maintaining control over critical points and preventing potential food safety hazards.

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6
Q

Define Audit

A

Systematic, independent examination to determine whether activities and related results comply with planned arrangements and whether these arrangements are implemented effectively and are suitable to achieve objectives.

  • Audits provide assurance of conformity and effectiveness of management systems.

Audits are conducted by qualified auditors and can be internal (self-assessment) or external (by third parties) to assess compliance with standards and regulatory requirements.

Audit findings help organizations identify opportunities for improvement and ensure compliance with legal, industry, and organizational requirements.

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7
Q

Define Corrections

A

Actions to eliminate detected nonconformities.

  • Corrections address immediate issues to prevent their recurrence.

Corrections may involve immediate corrective actions to mitigate risks or long-term preventive measures to improve processes and prevent similar issues.

Implementing timely and effective corrections is crucial for maintaining product quality, customer satisfaction, and regulatory compliance.

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8
Q

Define Standardization

A

Establishing, implementing, and maintaining standards to ensure consistency and uniformity in products, processes, or services.

  • Standardization promotes efficiency, quality, and interoperability.

Standardization involves developing agreed-upon guidelines, specifications, or criteria to streamline operations and enhance compatibility across industries or sectors.

Adopting standardized practices helps organizations achieve economies of scale, improve product quality, and facilitate market access and international trade.

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9
Q

Define PRPs (Pre-Requisite Programs)

A

Basic conditions and activities necessary to maintain a hygienic environment throughout the food chain and prevent food safety hazards.

  • PRPs include sanitation, pest control, personnel hygiene, and facility maintenance.

PRPs are foundational to food safety management systems, ensuring basic hygiene and operational conditions are met to minimize contamination risks.

Implementing effective PRPs is essential for preventing foodborne illnesses and ensuring compliance with food safety regulations and standards.

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10
Q

Define Reference Method

A

A standardized procedure or technique for performing measurements or tests.

  • Reference methods provide a basis for comparison and validation of results.

Reference methods are established to ensure consistency, accuracy, and reliability in analytical testing and scientific research.

Using reference methods helps laboratories and industries achieve traceable and comparable measurement results, supporting quality assurance and regulatory compliance.

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11
Q

Define Standard Reference Material

A

Certified material with known properties and characteristics used for calibration, validation, and quality control in analytical testing.

  • Standard reference materials ensure accuracy and traceability of measurement results.

Standard reference materials are used as benchmarks in analytical chemistry, metrology, and quality control to validate measurement instruments and methods.

Maintaining accurate and traceable measurements with standard reference materials supports confidence in analytical results and facilitates international trade and regulatory compliance.

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12
Q

Define Reproducibility

A

The degree of agreement between independent test results obtained under stipulated conditions.

  • Reproducibility measures the consistency of results when tests are repeated.

Reproducibility assessments evaluate the variability and reliability of measurements or experimental outcomes under controlled conditions.

Enhancing reproducibility in research and testing ensures reliability and confidence in scientific findings and technological developments.

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13
Q

Define Limit of Detection (LoD)

A

The lowest concentration or amount of a substance that can be reliably distinguished from the absence of that substance.

  • LoD is determined with a specified degree of confidence under defined experimental conditions.

LoD is crucial in analytical chemistry, environmental testing, and food safety to ensure accurate detection and quantification of contaminants or analytes.

Knowing the LoD helps laboratories establish detection capabilities and set appropriate thresholds for compliance and risk management.

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14
Q

Define Food Security

A

Ensuring that all people, at all times, have physical, social, and economic access to sufficient, safe, and nutritious food that meets their dietary needs and food preferences for an active and healthy life.

  • Food security encompasses availability, access, utilization, and stability of food sources.

Achieving food security requires sustainable agricultural practices, equitable distribution, and poverty alleviation efforts to meet global nutritional needs.

Addressing food security challenges involves policies and interventions to improve food access, affordability, and nutritional diversity for vulnerable populations worldwide.

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15
Q

Define Critical Limit

A

The maximum or minimum value to which a biological, chemical, or physical parameter must be controlled at a CCP to prevent, eliminate, or reduce a hazard to an acceptable level.

  • Critical limits are established in HACCP systems to ensure food safety.

Setting critical limits is essential for maintaining control over CCPs and ensuring effective hazard management.

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16
Q

Define Audit

A

Systematic, independent examination to determine whether activities and related results comply with planned arrangements and whether these arrangements are implemented effectively and are suitable to achieve objectives.

  • Audits provide assurance of conformity and effectiveness of management systems.

Conducting audits helps identify areas for improvement and ensures compliance with standards and regulations.

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17
Q

Define Corrections

A

Actions to eliminate detected nonconformities.

  • Corrections address immediate issues to prevent their recurrence.

Implementing timely corrections is crucial for maintaining product quality and meeting customer expectations.

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18
Q

Define Standardization

A

Establishing, implementing, and maintaining standards to ensure consistency and uniformity in products, processes, or services.

  • Standardization promotes efficiency, quality, and interoperability.

Adopting standardized practices enhances market competitiveness and facilitates international trade and cooperation.

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19
Q

Define PRPs (Pre-Requisite Programs)

A

Basic conditions and activities necessary to maintain a hygienic environment throughout the food chain and prevent food safety hazards.

  • PRPs include sanitation, personnel hygiene, and facility maintenance.

Implementing PRPs is essential for establishing the foundation of food safety management systems, such as HACCP.

20
Q

Define Reference Method

A

A standardized procedure or technique for performing measurements or tests.

  • Reference methods provide a basis for comparison and validation of results.

Using reference methods ensures accuracy, reliability, and consistency in analytical testing and measurement.

21
Q

Define Standard Reference Material

A

Certified material with known properties and characteristics used for calibration, validation, and quality control in analytical testing.

  • Standard reference materials ensure accuracy and traceability of measurement results.

Using standard reference materials supports reliable and comparable measurements across laboratories and industries.

22
Q

Define Reproducibility

A

The degree of agreement between independent test results obtained under stipulated conditions.

  • Reproducibility measures the consistency of results when tests are repeated by different operators or in different laboratories.

Assessing reproducibility ensures reliability and confidence in analytical methods and measurement data.

23
Q

Define Limit of Detection (LoD)

A

The lowest concentration or amount of a substance that can be reliably distinguished from the absence of that substance.

  • LoD is determined with a specified degree of confidence under defined experimental conditions.

Knowing the LoD is crucial in analytical chemistry, environmental testing, and food safety to ensure accurate detection of contaminants or analytes.

24
Q

Define Food Security

A

Ensuring that all people, at all times, have access to sufficient, safe, and nutritious food to lead active and healthy lives.

25
Q

Define AOAC (Association of Official Analytical Chemists)

A

A nonprofit organization that develops standards and methods for analytical chemistry and laboratory practices.

  • AOAC methods are widely recognized and used for testing the composition, safety, and quality of foods, beverages, and other products.

AOAC’s standards ensure consistency and reliability in analytical testing across industries.

26
Q

Define GMB (General Management Body)

A

A governing body responsible for overseeing general management functions within an organization.

  • GMB typically includes executive management, administrative leaders, and other key decision-makers.

GMB establishes policies, strategies, and direction to achieve organizational objectives and ensure effective management.

27
Q

Define Linear Range

A

The range of values over which a measurement instrument provides accurate and reliable results.

  • Within the linear range, the instrument’s response is directly proportional to the quantity being measured.

Understanding the linear range helps ensure accurate measurements and reliable data interpretation.

28
Q

Define Positive Deviation

A

When actual performance or results exceed expected or target values.

  • Positive deviations indicate superior performance or unexpected improvements.

Analyzing positive deviations helps identify best practices and areas for further improvement within organizations.

29
Q

Define ISMS (Information Security Management System)

A

A systematic approach to managing sensitive company information to ensure its confidentiality, integrity, and availability.

  • ISMS frameworks, such as ISO 27001, help organizations protect valuable information assets.

Implementing ISMS safeguards against information security threats and vulnerabilities, maintaining trust and compliance with legal and regulatory requirements.

30
Q

Define ISO Guide-65

A

A former international standard (replaced by ISO/IEC 17065) that provided requirements for bodies certifying products, processes, and services.

  • ISO Guide-65 outlined criteria for competence, consistency, and impartiality of certification bodies.

ISO Guide-65 aimed to ensure the reliability and credibility of certifications worldwide.

31
Q

Define Validation

A

Confirmation through provision of objective evidence that the requirements for a specific intended use or application have been fulfilled.

  • Validation ensures that processes or systems consistently produce desired outcomes.

Validating processes is essential in ensuring product quality, safety, and regulatory compliance.

32
Q

Define Accreditation

A

“Formal recognition that a body or person is competent to perform specific tasks.

33
Q

Define Requirements

A

Specifications or criteria that must be met or satisfied.

  • Essential for ensuring products, services, or processes fulfill their intended purpose and meet customer needs or regulatory obligations.

Requirements are fundamental in quality management systems to establish clear goals and expectations.

34
Q

Define Hazard

A

A potential source of harm or adverse health effect on humans, property, or the environment.

  • Hazards can arise from biological, chemical, physical, ergonomic, or psychosocial factors.

Understanding hazards is crucial in risk assessment and management to ensure safety and compliance.

35
Q

Define Audit Scope

A

The defined boundaries, objectives, and criteria for an audit.

  • Specifies what aspects of an organization, system, or process will be examined during the audit.

Audit scope helps ensure audits are focused and comprehensive, addressing specific areas of concern.

36
Q

Define Standard

A

A documented agreement containing technical specifications or other precise criteria.

  • Standards ensure consistency and quality in products, processes, or services.

Adherence to standards is critical for meeting customer expectations and regulatory requirements.

37
Q

Define Quality Assurance

A

Planned and systematic activities implemented to ensure that products or services meet specified requirements.

  • Includes quality control, quality planning, and continuous improvement processes.

Quality assurance aims to enhance customer satisfaction and confidence in the organization’s products or services.

38
Q

Define Record

A

Documentary evidence of activities performed or results achieved.

  • Records provide traceability, accountability, and documentation of compliance.

Proper record-keeping is essential for audits, regulatory compliance, and continuous improvement.

39
Q

Define Attestation

A

A declaration or statement confirming the truth or accuracy of something.

  • Often provided by a competent authority or through formal certification processes.

Attestation ensures credibility and reliability in statements or claims made by organizations or individuals.

40
Q

Define CCP (Critical Control Point)

A

A specific point where control can be applied to prevent, eliminate, or reduce a food safety hazard to an acceptable level.

  • Critical in Hazard Analysis Critical Control Point (HACCP) systems for ensuring food safety.

Identifying CCPs is crucial for managing risks and ensuring safe food production processes.

41
Q

Define PDCA (Plan-Do-Check-Act)

A

A four-step management method for continuous improvement: Plan, Do, Check, Act.

  • PDCA is used to achieve and maintain high-quality processes, products, or services.

PDCA fosters a culture of continual improvement and proactive problem-solving within organizations.

42
Q

Define IAF (International Accreditation Forum)

A

A global association of accreditation bodies.

  • IAF promotes consistency and mutual recognition of accredited conformity assessment results.

Membership in IAF ensures that accreditation practices meet international standards and best practices.

43
Q

Define NBQP (National Board of Quality Promotion)

A

A national body responsible for promoting quality management practices, standards development, and accreditation of conformity assessment bodies within a country.

  • NBQP plays a vital role in enhancing national quality infrastructure and competitiveness.

NBQP’s activities contribute to improving product and service quality across various sectors in the country.

44
Q

Define EMS (Environmental Management System)

A

A framework used by organizations to manage their environmental responsibilities in a systematic manner.

  • EMS helps organizations minimize their environmental impacts and comply with regulations.

Implementing EMS demonstrates an organization’s commitment to environmental stewardship and sustainability.

45
Q

Define Food Chain

A

The sequence of stages involved in the production, processing, distribution, and consumption of food products, from farm to table.

  • Includes agricultural practices, food processing, transportation, storage, retailing, and consumption.

Ensuring food safety and quality throughout the food chain is essential for protecting public health and meeting consumer expectations.

46
Q

Define Calibration

A

Comparing measurement values with a standard to ensure accuracy.

  • Calibration is essential for maintaining the reliability and consistency of measurement instruments.

Accurate calibration ensures that measurements are trustworthy and meet specified requirements.