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    產品詳細說明
    Introduction
    These guide?‌‌lines are intended to provide guidance regarding Good Manufacturing Practices for
    cosmetic products. These guidelines have been prepared for consideration by the cosmetic
    industry and take into account the specific needs of this sector. These guidelines offer
    organi...更多Introduction
    These guide?‌‌lines are intended to provide guidance regarding Good Manufacturing Practices for
    cosmetic products. These guidelines have been prepared for consideration by the cosmetic
    industry and take into account the specific needs of this sector. These guidelines offer
    organizational and practical advice on the management of the human, technical and administrative
    factors affecting product quality.
    These guidelines have been written to allow them to be used following the flow of products from
    receipt to shipment. Additionally, in order to clarify the way this document reaches its objectives, a
    ‘principle’ is added to each major section.
    Good Manufacturing Practices constitute the practical development of the quality assurance
    concept through the descrtption of the plant activities that are based on sound scientific judgement
    and risk assessments. The objective of these GMP guidelines is to define the activities that enable
    you to obtain a product that meets defined characteristics.
    Documentation is an integral part of Good Manufacturing Practices.
    介 紹
    這份準則為化妝品良好生產規范做出指導,是適合化妝品行業并考慮了行業的具體要求,在人
    員,技術和影響產品質量的綜合因素方面提供了系統性的和實際性的建議。
    這個指導是為了讓員工遵守產品接收到裝運的流程下如何去利用資源。為了達到此目的,在每
    一個章節里都添加了“原則”這一欄。
    良好生產規范中的質量保證發展觀念是通過描述建立在科學有效的判定和風險評估上的工廠活
    動來完成的,這份準則的目的是為了界定能讓你獲得達標產品的活動。
    文件是 GMP 不可或缺的一部分。
    4
    ISO22716:2007(E)
    化妝品良好生產規范準則
    1 Scope 范圍
    This International Standard gives guidelines for the production, control, storage and shipment of cosmetic products
    此國際標準為化妝品生產,控制,儲存和裝運提供指南
    These guidelines cover the quality aspects of the product, but as a whole do not cover safety aspects for the personnel
    engaged in the plant, nor do they cover aspects of protection of the environment. Safety and environmental aspects are
    inherent responsibilities of the company and could be governed by local legislation and regulation.
    這個標準包含產品質量的各個方面但不包括員工安全和對環境的保護方面,安全和環境保護是公司的應的責任,可
    以通過當地的法律和法規加以管制
    These guidelines are not applicable to research and development activities and distribution of finished products.
    這些準則并不適用于設計和開發和產品營銷活動。
    2 Terms and definitions 術語和定義
    For the purposes of this document, the following terms and definitions apply.
    以下術語和定義對于本文件是適用的
    2.1 acceptance criteria 接收標準
    numerical limits, ranges, or other suitable measures for acceptance of test results
    數值限度,范圍或者其他可作為接受測試結果的方法
    2.2 audit 審核
    systematic and independent examination to determine whether quality activities and related results comply with planned
    arrangements and whether these arrangements are implemented effectively and are suitable for achieving objectives
    為獲得審核證據并對其進行客觀評價,以確定滿足審核準則的程度而進行的 系統的、獨立的、形成文件的過程。
    2.3 Batch 批
    defined quantity of raw material, packaging material or product issued from one process or series of processes so that it
    could be expected to be homogeneous
    從某個或多個操作獲得的、認為是一致的特定數量的原料,包材或產品。
    2.4 batch number 批號
    distinctive combination of numbers, letters and/or symbols, which specifically identifies a batch
    單個數字,字母,或字母和數字結合的,用來指定識別一批產品的代碼.
    2.5bulk produc 散裝產品
    any product which has completed manufacturing stages up to, but not including, final packaging
    經過所有制造工藝過程的產品,除了沒有填充到獨立包裝的產品。
    2.6Calibration 校準
    set of operations that establish, under specified conditions, the relationship between values indicated by a measuring
    5
    6
    instrument or measuring system, or values represented by a material measure, and the corresponding known values of a
    reference standard
    在特定條件下,通過一系列操作在測量儀器或測量系統所指示的量值,或事物量具或參考事物表示的值,和按標準
    實現的相應值間建立起一種關系。
    2.7 change control 變更控制
    internal organization and responsibilities relative to any planned change of one or several activities covered by the Good
    Manufacturing Practices in order to ensure that all the manufactured, packaged, controlled and stored products correspond
    to the defined acceptance criteria
    為確保生產,包裝,控制,儲存符合接收標準,組織所作的內部機構、職責與 GMP 內容有關的任何計劃的變動。
    2.8Cleaning 清洗
    all operations that ensure a level of cleanliness and appearance, consisting of separating and eliminating generally visible
    dirt from a surface by means of the following combined factors, in variable proportions, such as chemical action,
    mechanical action, temperature, duration of application
    為確保達到潔凈水平,隔離或消除表面贓物的所有操作。例如用化學作用,機械作用,溫度,時間等方法。
    2.9Complaint 投訴
    external information claiming a product does not meet defined acceptance criteria
    外部信息斷言成品有質量缺陷。
    2.10Contamination 接觸污染
    occurrence of any undesirable matter such as chemical, physical and/or microbiological matter in the product
    指在產品中發現任何不應出現化學的,物理的,生物的物質的事件。
    2.11Consumables 耗材
    materials such as cleaning agents and lubricants that are used up during cleaning, sanitization ormaintenance operations
    指某些在清潔、**或維護中消耗的材料諸如清潔劑、潤滑油等。
    2.12contract acceptor 受托方
    person, company or external organization carrying out an operation on behalf of another person, company or organization
    代表某人、公司、組織實施操作的個人、公司或外部的組織。
    2.13
    Control 控制
    verification that acceptance criteria are met 確認可接受準則得到滿足
    2.14
    Deviation 偏差
    internal organization an

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