In the personal lubricant market, consumer demands for product quality and safety are increasingly high. When it comes to high-quality production, GMP (Good Manufacturing Practice) standards are an unavoidable keyword.
Although Personal Lubricant may be classified as cosmetics or Class II medical devices in some regions, if they can be produced according to the more stringent GMP standards, their products undoubtedly possess significant advantages in multiple dimensions. So, what exactly makes Personal Lubricant produced under GMP standards "good"?
Firstly,it's source-level safety assurance. GMP standards have extremely strict regulations for the procurement, acceptance, storage, and use of raw and auxiliary materials. This means factories will prioritize high-purity, medical-grade raw materials and conduct strict audits of suppliers, fundamentally preventing non-compliant or potentially risky substances from entering the production chain, ensuring product purity and mildness.
Secondly, it's a refined control of the production process. GMP requires the production environment to reach a certain level of cleanliness, such as being equipped with 100,000-class or even higher-grade dust-free cleanrooms, effectively preventing microbial and dust contamination. At the same time, there are clear and detailed specifications for production equipment, process flows, operator qualifications, hygiene conditions, etc., ensuring every production link is carried out under controlled conditions, minimizing the risk of cross-contamination and operational errors.
Thirdly, it's a comprehensive quality management system. GMP emphasizes a quality management philosophy of full participation and comprehensive control. From product design and development, manufacturing, quality inspection, finished product release, storage, and transportation, to adverse reaction monitoring and product recall, there is a complete documented system and SOPs (Standard Operating Procedures) to guide and record, ensuring product quality stability and traceability. This means every batch of product is traceable, and any problems can be quickly located and resolved.
Fourthly, it's a high guarantee of product batch stability. Through standardized operations and strict quality control, GMP production can ensure that different batches of products maintain high consistency in active ingredient content, physicochemical properties (such as pH value, viscosity), and microbial limits, providing consumers with a consistently high-quality experience.
PINGCHUANG MEDICAL's production base strictly implements GMP pharmaceutical production standards, equipped with a 16,000-square-meter modern factory and a 3,000-square-meter 100,000-class dust-free cleanroom. This is not only a commitment to high quality but also a responsibility for consumer safety.
