Why passing the lab is not enough
The source article opens by challenging a familiar assumption in biological-product manufacturing: quality cannot be measured by marketing claims or a few COA figures alone.
It points out that some products may technically pass laboratory checks yet still underperform in real farm conditions because QA and QC stop at paperwork compliance instead of evaluating scientific substance and biological effect.
What a strong QA and QC team must do
Than Vuong positions QA and QC as an active scientific function with responsibilities that reach far beyond checking numbers or comparing results against a fixed checklist.
- Understand product mechanisms in depth, including how functional ingredients interact with microbial membranes, biofilms, and resistant bacterial pressure.
- Control risk at the source by identifying weaknesses in raw materials, manufacturing, stability, and biological compatibility before problems reach the market.
- Evaluate true use-value so the product performs not only during storage and circulation, but also under real field conditions such as shrimp ponds and livestock operations.
QA and QC as the bridge between lab, production, and use
The article describes strong QA and QC as the protector of a product's scientific integrity and the bridge linking the laboratory, manufacturing operations, and practical use.
In the context of rising antimicrobial resistance, it argues that only companies with technically accountable QA and QC teams can consistently ship products that remain stable, safe, and effective.
Why this matters for long-term growth
The closing argument is straightforward: deeper QA and QC capability is not only a factory function. It is a trust-building system that protects reputation, strengthens market confidence, and creates a more durable platform for growth in modern aquaculture and bioscience.