Cosmetic clean workshop inspection and reagent management
Cosmetic clean workshop inspection and reagent management
Cosmetics production enterprises should establish inspection standards for raw materials, packaging materials, intermediate products and products. Enterprises should comprehensively consider the raw material data provided by suppliers, relevant national standards, industry standards and product research and development data, and formulate raw material standards, such as raw materials the pure...
Text label: Cosmetics clean pharmaceutical cleanroom, inspection and reagent management, design, installation and construction
Cosmetics clean workshop inspection and reagent management
Cosmetics production enterprises should establish inspection standards for raw materials, packaging materials, intermediate products and products. Enterprises should comprehensively consider the raw material data provided by suppliers, relevant national standards, industry standards and product research and development data, and formulate raw material standards, such as raw materials The purity, metal content, microbial requirements, etc., some of these requirements are also reversed according to the final product requirements, and the result is to ensure product quality. Cosmetic clean pharmaceutical cleanroom packaging materials are divided into inner packaging materials and outer packaging materials. The inner packaging material is the packaging material that directly contacts the contents of the product. Generally, functional and safety indicators should be paid attention to, such as compatibility with the product, sealing, reactivity, etc., other Items such as specifications, appearance, structure, etc. also need to be specified; outer packaging generally pays attention to appearance, size, color and label content, etc., and the inner and outer packaging should be consistent in the printed content.
Semi-finished products produced in the production process of cosmetic clean workshops, such as semi-finished products in the batching process and semi-finished products in the sub-packaging process, the semi-finished products in the sub-packaging process focus on label content, net content, sealing, etc.; semi-finished products in the batching process generally pay attention to appearance and smell , PH value, viscosity, microbial content and other indicators. Finished product standards, the state has specific regulations on cosmetic standards. Enterprises can directly refer to the implementation standards on product labels as finished product standards, or they can formulate internal control standards that are stricter than this implementation standard, but the testing items are generally the same, including appearance, PH value , net content, cold resistance, heat resistance, microorganisms, packaging sealing and heavy metal content, etc.; the enterprise should make reasonable regulations on the testing items and testing frequency in the standard, and sampling according to the specified method to ensure that the samples are representative, such as sampling The quantity, sampling location, unpacking rate and sampling process should be specified to avoid deviations caused by different operating habits of different personnel; the samples taken should be clearly marked to avoid confusion, such as the sample name, batch number, The sampling date, sampling quantity, sampling person, etc., the samples should also be stored in accordance with the specified conditions. For example, some samples need to be controlled in storage temperature and humidity, some need to be stored away from light, and some need to be sealed and stored because they are easy to absorb water or volatilize. Zhongjing Global Purification can provide consulting, planning, design, construction, installation, transformation and other supporting services for cosmetic production workshops and clean workshops.
Reagents, test solutions and culture medium are just as important for enterprise testing as raw materials and packaging materials are in the production process, and the management of reagents is very important. Enterprises should manage reagents, test solutions and culture medium according to regulations; Once the reagents are purchased, they must be stored in accordance with the specified conditions to ensure that they will not fail due to storage conditions. Although some reagents have a longer validity period, they also stipulate that they can only be valid for a short period of time once they are opened. It is five years. After opening, it can only be guaranteed to be valid for one year, and the one-year validity period is also based on the fact that the reagent has been kept at the specified temperature. In this case, enterprises should pay special attention. The prepared standard solution and culture medium must be clearly marked, including but not limited to the name, batch number, preparer, preparation date, expiration date and concentration, etc. The prepared standard solution and culture medium must keep preparation records, Record in detail the name, batch number, and preparation process of the stock solution used for preparation. The preparation records should be properly kept and the traceability of the entire process should be retained.
SUZHOU PHARMA MACHINERY CO.,LTD. is different from other companies as we provide timely and unique services to our respected clients.
SUZHOU PHARMA MACHINERY CO.,LTD. is working with the best teams, aligned with international standards and practices to focus on R&D and manufacture of products, and are continuously launching new products in the market. Get to know us at PHARMA MACHINERY.
In various different types of extraction machine, extraction machine CUSTOM SOLUTION SERVICES is one of the most commonly used.
SUZHOU PHARMA MACHINERY CO.,LTD. provides a way for you to understand your customers, to learn what makes them unique and what motivates their behavior. We can then leverage that wealth of information to personalize our interactions and demonstrate that CUSTOM SOLUTION SERVICES is valuable to our customers.