Prelim quiz Flashcards
This should be calibrated regularly and placed accordingly to facilitate efficient production of cosmetics.
Documentation
Personnel
Buildings
Equipments
Equipments
They should be in good health, well-trained and skilled.
Equipment
Head of Production
Buildings
Personnel
Personnel
Which document lists the raw materials used in most cosmetics around the world?
International Nomenclature of Cosmetic Raw Materials
International Nomenclature of Cosmetic Ingredients Dictionary
International Nomenclature of Cosmetic Directive
International Nomenclature of FDA Cosmetic Regulation
International Nomenclature of Cosmetic Ingredients Dictionary
Technology that is promising to cosmetic science that activates DNA sequences based on environmental conditions.
Microbial cleansing
3D printing
Plant resources
Epigenetics
Epigenetics
Technology that is promising to cosmetic science that uses good microbes to clean skin surface.
Microbial cleansing
Plant sources
3D printing
Epigenetics
Microbial cleansing
This should be developed, established and implemented as a means by which stated policies and objectives will be achieved. It should define the organizational structure, functions, responsibilities, procedures, instructions, processes and resources for implementing the quality management.
Quality Management System
Cosmetic Manufacturing Process
Cosmetic Good Manufacturing Practice
Continuous Improvement
Quality Management System
This should be suitably located, designed, constructed and maintained.
Equipment
Documentation
Personnel
Premises
Premises
Which of the following can be employed to prevent cross-contamination and and risk of mix-up?
Flexible barrier
Toilets near production area for easier cleaning
Duct tape
Blackout curtains
Flexible barrier
The following measures with regards to buildings should be observed in accordance to Cosmetic GMP, EXCEPT:
It should be installed appropriately
Adequately lit
Able to support the operations of the company
Well-ventilated
It should be installed appropriately
The following measures should be observed by personnel pertaining to sanitation and hygiene, EXCEPT:
Suitable locker facilities
Avoidance of eating and drinking in the production area
Regular medical examination
Practice good personal hygiene
Suitable locker facilities
This is an important starting material thus rigorous testing should be employed such as chemical and microbiological testing. Methods of treatment include deionization, distillation and filtration.
Lactose
Water
Talc
Starch
Water
This serves as an identification to products and for traceability.
Batch Numbering System
Expiration date
Documentation
Manufacturing Date
Batch Numbering System
The following are measures employed in handling wet products, EXCEPT:
Dust-containing production system
Pipelines should be cleaned at all times
Closed systems
Protection from microbial contamination
Dust-containing production system
This should be taken and checked at random during labeling and packaging operations.
Samples
Lot
Calibration
Records
Samples
This is an essential part of GMP. It provides assurance that cosmetic products will be of consistent quality appropriate to their intended use.
Regulatory
Quality Assurance
Quality Control
Documentation
Quality Control
This consists of an examination and assessment of all or part of a quality system with the specific purpose of improving it.
Internal Audits
External Audit
Accreditation
Quality Control
Internal Audits
There should be a written contract between the principal and the another manufacturer to clearly establish the duties and responsibilities of each party.
Secondary Manufacturing
Tertiary Manufacturing
Primary Manufacturing
Contract Manufacturing
Contract Manufacturing
A quantity of any cosmetic product produced in a given cycle of manufacture that is uniform in character and quality.
Batch
Bulk Product
Lot
Sample
Batch
Combination of checking an instrument and adjusting it to bring it within its limits for accuracy according to recognized standards.
Weighing
Assay
Calibration
Testing
Calibration
All written procedures, instructions and records involved in the manufacture and quality control of products.
Documentation
Standard Operating Procedure
Master Formula
Batch Manufacturing Record
Documentation
A product which has undergone all stages of manufacturing operations.
Starting Material
Bulk Product
Finished Product
Intermediate Product
Finished Product
Any processed substance or mixture of substances which has to undergo one or more stages of processing to become a bulk product.
Intermediate Product
Finished Product
Starting Material
Bulk Product
Intermediate Product
The status of materials or products set apart physically or by system, while awaiting a decision for their rejection or release for processing, packaging or
distribution.
Rejected
Released
Approved
Quarantine
Quarantine
The status of materials or products which are allowed to be used for processing, packaging or distribution.
Released
Rejected
Approved
Quarantine
Released
