2025年3月7日 · GMP stands for Good Manufacturing Practices, a system that ensures that manufactured products—such as food, cosmetics, and pharmaceutical goods—are consistently produced and controlled according to set quality standards. Implementing GMP can help cut losses and waste, and avoid recalls, fines, and jail time.

2024年6月6日 · GMP SOPs are defined as written instructions that detail how to perform a task or process in a GMP-regulated manufacturing environment. Their primary purpose is to ensure that all operations are carried out consistently and correctly, …

Every pharmaceutical and medical device manufacturer should aim to operate their business following the principles of Good Manufacturing Practice (GMP) and it’s much easier to be GMP compliant if the design and construction of the facilities and equipment are right from the start.

2024年4月23日 · Let’s dive into the 10 basic principles of GMP. 1. Create Standard Operating Procedures (SOPs) The first of the 10 GMP principles is to create detailed, written SOPs for each process that could impact the quality of the final product. These SOPs will help streamline processes and ensure compliance with the desired quality standards. 2. Follow SOPs.

2024年10月30日 · This guide to good manufacturing practices (GMP) for manufacturers breaks down the essential principles, regulations, and actionable steps to implement GMP effectively. From maintaining cleanliness to ensuring product safety, learn how to meet the highest quality standards in your industry.

GMP covers all aspects of the manufacturing process: defined manufacturing process; validated critical manufacturing steps; suitable premises, storage, transport; qualified and trained production and quality control personnel; adequate laboratory

We offer clear, authentic, easy-to-follow standard operating procedures (SOP) for small and medium-sized pharmaceutical companies. Our SOPs comply with international standards like Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Good Distribution Practices (GDP), and Good Automated Manufacturing Practices (GAMP).

This guide covers the fundamentals of Good Manufacturing Practices (GMP), the 10 key elements for compliance, the GMP process, best practices, and FDA inspection insights.

2024年9月1日 · Let's delve into the key steps that pharmaceutical companies follow to ensure GMP compliance effectively. Step 1: Understand GMP Requirements. GMP regulations outline the standards for the design, monitoring, and control of manufacturing processes and facilities.

《药品生产质量管理规范》（Good Manufacturing Practice of Medical Products，GMP）是药品生产和 质量管理 的基本准则，适用于药品制剂生产的全过程和 原料药 生产中影响成品质量的 关键工序。 大力推行药品GMP，是为了最大限度地避免药品生产过程中的污染和交叉污染，降低各种差错的发生，是提高药品质量的重要措施。 世界卫生组织，60年代中开始组织制订药品GMP，中国则从80年代开始推行。 1988年颁布了中国的药品GMP，并于1992年作了第一次修订。 十几 …