SEMINAR: ISO/IEC17025/GLP

Welcome

Welcome speech

Assoc. Prof. Dr. Trinh Van Lau - Chairman of the Vietnam Pharmaceutical Enterprises Association

Ensuring Data Integrity and International Recognition: The Role of ISO 17025 and OECD GLP

Master Vu Minh Vy, Chief Evaluation Expert, National Accreditation Bureau

The new requirements in WHO TRS 1052 “WHO good practices for pharmaceutical quality control laboratories”. Developing a modern pharmaceutical microbiology laboratories, in accordance with international standards

Master Nguyen Thi Thu Huong, Deputy Head of the Microbiology Department, National Institute for Drug Quality Control

Design and construction of factories meeting GLP

Mr. Đào Xuân Hưởng – General Director of GMPc Vietnam

Teabreak

Sharing the practical implementation of GLP according to EU standards

Ms. Nguyễn Thị Kim Anh - Head of Quality Control Department, Stellapharm Joint Venture Company Limited

Sharing the current situation of developing national standards, national technical regulations, and intellectual property in science and technology and innovation in the field of research and development (R&D) and pharmaceutical and healthcare production.

Dr. Nguyen The Hung – Director of the VABIOTECH High-Tech Development Research Center

Elevating Vietnamese laboratories: From international standards to efficient operation.

Mrs. Nguyen Thi Thanh Man, Supply chain management, CHC Lab Vietnam

Panel Discussion: ISO/IEC17025/GLP - From Regulations to Application and Practical Experiences

Assoc. Prof. Dr. Trinh Van Lau - Chairman of the Vietnam Pharmaceutical Enterprises Association