Inside Fivevet’s Veterinary Drug Manufacturing Facility - From Raw Materials to Finished Products (Part II)

Continuing from Inside Fivevet’s Veterinary Drug Manufacturing Facility: From Raw Materials to Finished Products (Part I) (Chèn link phần 1), Fivevet will introduce finished product testing, its QA/QC system, and storage requirements in Part II, explaining how these help maintain product quality before products reach partners and customers.  5. Finished Product Testing: Each Dosage Form Has Its Own Specifications
Once manufacturing is complete, finished products are tested against their respective quality specifications. Tests include identification, active ingredient assay, impurities, dosage form properties, and microbiological testing, depending on the applicable requirements.
Test results are one of the factors used to assess a drug batch’s quality before it is approved for release.
In addition to finished products, Fivevet tests incoming raw materials, primary packaging that comes into direct contact with the drug, and intermediate products during manufacturing, helping control quality at each stage.
Read more: Veterinary Drug Testing Before Export at Fivevet: From Test Samples to Test Reports 
6. Fivevet’s QA/QC System and Quality Control Before Batch Release
At Fivevet, finished product testing is connected with the quality assurance system to control products throughout manufacturing, from incoming raw materials to batch release approval.
QC generally focuses on:
- Sampling.
- Quality specifications.
- Testing.
- Analytical methods.
- Evaluation of results.
QA has a broader scope, covering the entire quality assurance system.
A product batch should not be approved for release solely because its finished product test results meet specifications. The authorized person or department also needs to review:
- Manufacturing records.
- Packaging records.
- Test results.
- In-process controls.
- Deviations and related investigation findings.
- The completeness of batch records.
Out-of-specification test results need to be investigated and assessed according to appropriate procedures before decisions are made about the product batch.
Combining finished product testing with a review of manufacturing records and other relevant quality information gives Fivevet a basis for assessing each batch as a whole, rather than relying on a single test result.
For international importers and distributors, the QA/QC system and the ability to trace production batch information are important factors when assessing a manufacturer’s quality management capabilities and suitability for a long-term partnership.
7. Product Stability Control and Storage at Fivevet
Veterinary pharmaceuticals must meet quality specifications at release and maintain that quality throughout their shelf life when stored under the specified conditions.
At Fivevet, manufacturing is connected with storage facilities that meet WHO-GSP standards, helping maintain storage conditions suited to the requirements of each product group while in storage.
Stability study data also play an important role in establishing and assessing:
- Shelf life: Providing a scientific basis for determining how long a product maintains its quality attributes within the applicable specifications.
- Storage conditions: Identifying temperature, humidity, or other product-specific storage requirements.
- Packaging selection: Assessing whether packaging materials and specifications are suitable for protecting product quality.
- Distribution conditions: Providing a technical basis for reviewing storage and transportation requirements during distribution.
8. Fivevet – A Veterinary Pharmaceutical Manufacturing and Supply Partner for International Markets
With 15 production lines that meet WHO-GMP standards, Fivevet has developed the capacity to manufacture a range of veterinary drug dosage forms and vaccines, serving disease prevention and animal health care needs across multiple markets.
Manufacturing capabilities are connected with research, testing, quality management, and WHO-GSP storage facilities, providing a foundation for quality control from incoming raw materials to finished products.
With experience exporting products to more than 20 countries, Fivevet has developed a broad portfolio of veterinary solutions, from therapeutic drugs and vaccines to products supporting nutrition, animal health care, and biosecurity, serving the needs of international importers and distributors. Connect with Fivevet’s Export Team
Are you looking for a veterinary pharmaceutical manufacturer in Vietnam to expand your product portfolio or develop your distribution market?
Contact Fivevet’s export team to discuss the product range, technical documentation, packaging specifications, and partnership opportunities suited to your target market.
Email: export@fivevet.vn
Hotline/WhatsApp: +84 96 333 7900
Frequently Asked Questions
1. What Veterinary Drug Manufacturing Capabilities Does Fivevet Offer for Export Markets?
Fivevet’s manufacturing operations meet WHO-GMP standards and support a range of veterinary drug dosage forms. Manufacturing is connected with research, testing, and storage, helping control quality from incoming raw materials to finished products.
2. What Documentation Can Fivevet Help Provide for Veterinary Drug Importers?
Partners can discuss GMP documentation, quality specifications, CoAs, stability data, and technical documents for drug registration with Fivevet. The specific documents are determined by the product and the importing market’s requirements.
3. How Is the Quality of Each Export Drug Batch Controlled?
Before release approval, each drug batch needs to be reviewed based on its test results, manufacturing records, packaging records, and any related deviations. Partners can discuss finished product specifications and the test parameters reported on each batch’s CoA with Fivevet.
4. Can Fivevet Help Adapt Drug Packaging and Labels for the Importing Market?
Partners can work with Fivevet on packaging specifications, label content, and packaging requirements. These must align with the drug registration dossier and the importing market’s regulations before implementation.
5. What Information Should Importers Provide to Start Working with Fivevet?
Partners should provide the drug name or active ingredient of interest, dosage form, target market, and expected demand. Both parties can then agree on documentation, quality, packaging, and supply requirements. Contact Fivevet’s export team at export@fivevet.vn or +84 96 333 7900.
Read our detailed guide: Veterinary Medicine Distributor: 10 Criteria for Choosing the Right Manufacturer