ESG Report 2022

Relevant Laws, Regulations and Guidelines Criminal Law of the People's Republic of China Anti-Unfair Competition Law of the People 's Republic of China Interim Provisions on Banning Commercial Bribery The United Laboratories Employees' Code of Honesty and Self-Discipline The United Laboratories Anti-Fraud and Complaint Reporting Management System Statement of Integrity Anti-corruption Agreement Business ethics Realm The Group has established a clinical research plan, data management plan and risk control plan, centre. As a quality control system covering the and set clear provisions for reviewing, verifying and entire process of clinical trials, the centre is mainly tracing original data, frequency and requirements responsible for the clinical development strategy of inspections, collaborative monitoring, auditing, and path formulation, research protocol design, etc. Clinical trials shall ensure all subjects sign the clinical trial organization and implementation, informed consent forms through examination by the project management and monitoring, quality control drug clinical trial institution and ethics committee. and other related work for all clinical trial projects of the Group. Regarding the personal information security of the subjects, the company has always adhered to the During the reporting period, all clinical trials of the purpose of strictly protecting the data security of Group strictly complied with the Declaration of the subjects. We ensure the confidentiality of the Helsinki of the World Medical Association, the Civil research project data through confidentiality Code of the People's Republic of China, the Drug measures such as anonymization or coding, and Administration Law of the People's Republic of prevent the harm and risks caused by the leakage China, Measures for the Administration of Drug of the subjects' privacy. Registration, Quality Control of Clinical Trials of Drugs and Measures for Ethical Review of Life The Group is currently conducting 10 clinical trials Sciences and Medical Research Involving Humans for chemical and biological innovative drugs as well principles and related ethical requirements, taking as biosimilars. Besides, clinical trials of several the rights and safety of subjects as the primary innovative drugs and biosimilars are about to start. concern in drug clinical trials. We require all drug In the process, we will realise continuous clinical trials to obtain a clinical trial license, m o n i t o r i n g , i n s p e c t i o n , f e e d b a c k a n d develop scientific, ethical, compliant and practical improvements of the quality of clinical trials to clinical trial protocols and work plans, including but ensure the quality of clinical trials. not limited to project management plan, inspection 5.2.1 Medical Ethics Environmental, Social and Governance Report 2022 The United Laboratories International Holdings Limited 21