The Workshop on Assessment and Control of Clean Room Systems

“The Workshop on Assessment and Control of Clean Room Systems” is an event organized by LABone Scientific Equipment Company in Ho Chi Minh City on June 8-9, 2023. This workshop will help pharmaceutical experts understand the process of controlling clean room systems in the pharmaceutical industry, according to GMP WHO and ISO 14644:2022 standards.

The instructor for this workshop is Ths. Nguyen Thi Thu Huong, Deputy Head of Microbiology Department – Central Drug Testing Institute, with over 19 years of experience in clean room and microbiological testing.

➤ Deputy Head of Microbiology Department – Central Drug Testing Institute

➤ GMP Technical Inspection Expert

➤ Independent Technical Expert in the Pharmaceutical Industry – Vietnam Quality Accreditation Department (BoA)

➤ Pharmaceutical Organization Accreditation Evaluation Expert – Vietnam Quality Accreditation Institute

➤ 19 years of experience in clean room and microbiological testing

➤ 06 years of experience in teaching training courses: “Good practice in microbiological testing in the pharmaceutical industry”; “Assessment of clean room systems”; “Control of clean rooms”; “Assessment of pharmaceutical steam sterilizers”, etc.

 

The workshop ” Assessment and Control of Clean Room Systems – pharmaceutical field according to GMP WHO and ISO 14644:2022″ organized by LABone company, included both theoretical and practical parts. The theoretical part covered topics such as the design principles of clean rooms according to WHO TRS 961:2011; WHO TRS 1044:2022; ISO 14644:2022, the general structure of clean room systems, the principles of conducting IQ, OQ, PQ evaluation of new clean room systems, and methods for evaluating the technical indicators of clean rooms.

The practical part took place at LABone – Cu Chi factory. The participants were divided into 4 practical groups, each with 4 technical indicators including measuring airborne particles, checking microorganisms in the air and on surfaces, determining the leakage of HEPA filters, and measuring the velocity in Class A clean rooms.

The workshop also introduced a Q&A session in the field of clean rooms to address any questions or concerns of the participants.

With the emergence of infectious diseases such as COVID-19, controlling clean room systems in the pharmaceutical field has become increasingly important. This workshop was an excellent opportunity for experts in the pharmaceutical field to update their knowledge and skills in controlling clean room systems.

During the theoretical part, Ths. Nguyen Thi Thu Huong presented the design principles of clean rooms according to WHO and ISO 14644:2022 guidelines. In addition, the lecturer also introduced the general structure of clean room systems and methods for evaluating the technical indicators of clean rooms.

In the practical part, the participants were divided into 4 groups to practice with 4 different technical indicators. Each group performed tasks corresponding to their assigned technical indicator. This was a great opportunity for participants to gain hands-on experience and practical skills.

To help participants better understand the content presented in the workshop, the lecturer also provided a Q&A bank in the field of clean rooms. This helped participants clarify any doubts and improve their knowledge after the workshop.

Overall, the “Assessment and Control of Clean Room Systems – pharmaceutical field according to GMP WHO and ISO 14644:2022” workshop organized by LABone company provided valuable knowledge for participants. The training program included both theoretical and practical parts, giving participants the opportunity to gain practical experience and learn the necessary skills to control and evaluate clean room systems in the pharmaceutical field.

For more detailed information about the exhibition, please contact:

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