1st GMP – WHO veterinary medicine factory in Vietnam with 3 leading standards | Achaupharm

Achaupharm 1st GMP – WHO veterinary medicine factory in Vietnam In order to meet the increasing demand of the market and ensure the safety of animal health, the adherence to Good Manufacturing Practices (GMP) – World Health Organization (WHO) standards has become an important goal for veterinary medicine manufacturers in Vietnam.

1. What is a GMP-WHO compliant veterinary drug manufacturing plant?

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To achieve GMP-WHO standards, a veterinary drug and aquaculture manufacturing plant must meet the following three criteria:

I. Good Storage Practices (GSP):

GSP involves specific measures suitable for the storage and transportation of raw materials and products at all stages of production, storage, and drug preservation. This is to ensure that the finished product maintains its intended quality when it reaches the end consumer. To achieve GSP, manufacturers must establish and equip adequate storage facilities (cool storage, cold storage, controlled storage, etc.) for all stages from raw materials, primary packaging, secondary packaging, finished products, and for export.

II. Good Laboratory Practices (GLP):

GLP encompasses systematic and pre-planned activities in testing to ensure the necessary reliability and meet quality requirements. To achieve GLP, manufacturers must establish and equip facilities, machinery, equipment, personnel, and techniques to test all quality indicators (physical, chemical, and microbiological) related to product quality. This is carried out consistently from the workshop, production area, production machinery, raw materials, packaging, to the products for sale and the stability of the product when it enters the market.

III. Good Manufacturing Practices (GMP):

GMP consists of general regulations and guidelines to ensure that manufacturers can consistently produce products that meet quality standards and are safe for use. This is carried out consistently based on factors from the environment, raw materials, human resources, techniques, equipment, and implementation processes.

The application of GMP aims to help veterinary drug manufacturing plants comply with GMP-WHO standards by preventing or minimizing factors that affect drug quality during production such as disorder, confusion, or contamination. This is not only the responsibility of drug manufacturers but also falls under the government’s policy.

2. Achaupharm – 1st GMP – WHO veterinary medicine factory in Vietnam

Achaupharm takes pride in being a GMP-WHO compliant veterinary drug manufacturing plant with three production lines meeting international standards:

• Infrastructure: Ensuring that production, storage, and testing areas are in compliance with hygiene, safety, and environmental standards.
• Production Equipment: Modern equipment that ensures the accuracy and reliability of the production process.
• Production Processes: Standardized processes, from raw materials to finished products, ensuring product consistency and safety.
• Quality Control: Strict quality control procedures, from testing raw materials to final product inspection before leaving the factory.
• Production Record Management: Careful storage of production records that can be easily retrieved, ensuring transparency and compliance.

The application of GMP-WHO compliant veterinary medicine factory plant standards is not only a requirement but also an opportunity for Achaupharm to enhance product quality, expand its market, and increase its competitive value. Investing in compliance with GMP-WHO not only brings immediate benefits but also serves as a foundation for Achaupharm’s sustainable development in the future of the veterinary drug industry.

In conclusion, adhering to 1st GMP – WHO veterinary medicine factory in Vietnam is crucial for ensuring product quality and safety. Achaupharm’s commitment to meeting these standards reflects its dedication to providing high-quality veterinary drugs while contributing to the growth and development of the industry.

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