In October 2025, all Davipharm auditors and new candidates participated in the second advanced training session at our Binh Duong site office (HCMC), aimed at strengthening knowledge and meeting the latest requirements for GMP Auditors.

The session welcomed over 30 participants from key departments including Quality Assurance, Quality Control, Production, Packaging, Data Integrity, Regulatory Affairs, and Supply Chain, under the thorough guidance of Ms. Iskra-Jopa Joanna (Qualified Person).

The Validation Team shared valuable insights on processes of mapping, equipment evaluation and manufacturing…, while the Quality Control Team presented the expertise in physicochemical & microbiological practices.

The interactive Q&A encouraged participants to exchange practical solutions. Through this collaborative learning, Davipharm’s auditors continue to further strengthen their skills, ensuring the company remains compliant and committed to quality.