Pharmaceuticals
We support pharmaceutical manufacturers in being able to show, before production begins, that the raw materials and excipients they use match what is declared.
Do you verify at goods-in that the raw material entering production is the substance declared?
In pharmaceuticals the conformity of the raw material determines the whole finished product. That makes the moment the material enters the warehouse the point where a check is worth most.
- Supplier certificates of analysis arrive but no independent verification is done
- The source of excipients can change from batch to batch
- If a non-conformity is caught in the finished product the cost multiplies
- Audits ask for records of goods-in checks
What we provide to pharmaceutical manufacturers
A setup that puts your goods-in checks on record without touching your production.
Identity verification at goods-in
You see that raw material entering the warehouse is the substance declared, before it goes into production.
Excipient consistency
You track over time whether batches from the same supplier agree with one another.
Audit-ready records
The history of your goods-in checks stands ready when it is asked for.
What matters in pharmaceuticals
Three priorities in your industry.
Raw material responsibility
The conformity of every substance used sits with the manufacturer, certificate notwithstanding.
Supply chain depth
How many hands a raw material passed through is usually invisible.
Audit frequency
Goods-in check records are among the first headings a routine audit asks about.
Let's assess your goods-in checks together.
We will start from your supplier structure and your product range.