HANVET GMP-WHO FACTORY
Located in an area of 40,000 m2 at Pho Noi A Industrial zone,
My Hao commune, Hung Yen province, HANVET factory has successfully gone into
operation since 2008. Certified by GMP_WHO standards, we are producing a diversity
of dosage forms for the treatment and prevention of various infectious diseases
|Total factory area||
400 m2 x 3 floors
|GMP plant area||
|Auxiliary utilities (electric system, Generator, water system (soft water, RO water and distilled water), HVAC, boiler, Gas supplying system (O2, N2, gas), System for the treatment of liquid waste...||
|QA, QC, R&D||
|Building for Research and Production of Bio-product||
420 m2 x 3 floors
|Built up ground floor||
4,000 m2 (24,000m3)
|Non-GMP (insecticides and disinfectants)||
|Water area (ponds)||
1 000 m2
Our manufacturing licenses were issued in accordance with the Decision No.53/1999/QD/BNN-TCCB of Ministry of Agriculture and Rural Development and the Production Approval No. 055931 of Department of Planning and Investment of Hanoi City, dated April 19,1999
GOOD MANUFACTURING PRACTICE – GMP
General layout of our manufacturing process complies with
the flow of materials and personnels, in order to minimize risks of errors
and enhance effective cleaning and sanitation procedures.
In accordance with GMP-WHO standards, HANVET is now operating 05 production lines, which includes:
- Injectable solution and oral liquid.
- Injection powder.
- Powder, granules and tablets for oral administration.
- Topical preparations.
- Inactivated vaccines.
GOOD LABORATORY PRACTICE – GLP
The laboratory has been designed and equipped with facilities for chemical, physical, microbiological and stability testing. Temperature in the instrumental room is always kept under control. Microbiological area is constructed as per the clean-room principles of D-level, provided with laminar airflow as well as other facilities to carry out tests, assays, water testing and environment monitoring.
The microbiological laboratory is handled by a team of qualified microbiologists, who have both experience and expertise in carrying out bio-burden monitoring, microbial counts, pathogen characterization, microbiological analysis of water and materials.
GOOD STORAGE PRACTICE – GSP
The storage area is well maintained and equipped with air-conditioners to keep products in good conditions. Pharmaceutical water has been automatically produced with a capacity of 3,000 liters of soft water; 1,000 liters of RO water; and 300 liters of distilled water per hour on a continuous basis. All the toilets are integral with automatic flush. The whole facility is well maintained at all times with adequate and prompt repairs, re-paintings and services.