All Staff Study Legal Guidelines to Uphold Standards and Strengthen Drug Quality Control | A Record of Focusfreda's Legal Awareness Campaign
To thoroughly implement the legal education requirements of the Provincial Drug Administration and comprehensively promote the enforcement of the newly revised Implementation Regulations of the Drug Administration Law of the People's Republic of China, Focusfreda organized a series of specialized legal awareness campaigns from May to June 2026 to further strengthen compliance management throughout the entire drug production process. Centered on the objectives of "fostering a supportive environment, extensive dissemination, and in-depth learning," these initiatives employed multi-level, comprehensive legal education measures to ensure thorough understanding of relevant laws and regulations, thereby solidifying the quality and safety safeguards in drug production.
1. Coordinate deployment efforts, ensure comprehensive implementation, and foster a strong atmosphere for legal education.
To ensure the orderly implementation and tangible outcomes of legal awareness initiatives, the company has established a comprehensive plan for the entire campaign. Li Xiaojun, Deputy General Manager and Quality Director of Focusfreda, emphasized the significance of these efforts, defined specific job responsibilities, clarified operational requirements, and ensured thorough execution across all levels and involving all employees. Additionally, the company leveraged offline promotional channels—including hanging banners and setting up quality culture display boards—to consistently promote compliance in pharmaceutical production and the importance of lawful operations, fostering an environment where all staff actively study, understand, and adhere to legal standards.




II. Engage at the grassroots level, conduct regular legal education campaigns, and establish a sustainable mechanism for legal learning
Legal awareness campaigns have been deeply integrated into frontline operations and daily routines, with Focusfreda closely linking legal education with practical production needs. Each team utilizes pre-shift meetings as a platform to conduct legal awareness lectures and educational activities, focusing on operational standards and guidelines specific to their roles. This helps frontline employees clearly understand compliance requirements, identify operational boundaries, and uphold safety standards. By establishing a sustainable management mechanism of "learning regulations before shifts and adhering to compliance at workstations," the company ensures standardized, safe, and controllable production processes, fostering a strong culture of compliance across all positions.

III. Specialized Training: Strengthening Foundations and Ensuring Compliance Standards for All Employees
Led by the Organization's Human Resources Department, the company conducted a comprehensive training program for all employees on the "Regulations" and an excerpt of legal provisions regarding data reliability that frontline pharmaceutical production personnel must understand and master. Through systematic and professional instruction, this initiative significantly enhanced employees' ability to comprehend, adhere to, and apply legal requirements, thereby providing robust talent support and institutional safeguards for drug quality and safety, data compliance, and standardized production practices.


Next, Focusfreda will leverage this specialized legal awareness campaign as an opportunity to further advance the normalization, institutionalization, and standardization of legal education. We remain steadfast in upholding the fundamental principles of drug quality and safety, integrating legal compliance considerations throughout the entire process—from drug production and quality control to daily management—and continuously refining our compliance management system. By enhancing compliance standards, we aim to empower enterprises' high-quality development, effectively safeguard drug quality and safety, and fulfill the responsibilities and commitments inherent in pharmaceutical raw material manufacturers.
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