Have you ever wonder why automated inspection is no longer optional and how Automatic Tablet and Capsule Inspection Machines became a necessity?
In modern pharmaceutical manufacturing, quality control isn’t just a regulatory checkbox — it’s a competitive advantage. With increasing pressure from regulators like the US FDA, EMA, and CDSCO, manual inspection methods are fast becoming obsolete. This has led to the rise of the automatic tablet and capsule inspection machine.
— a smart, camera-based system that identifies visual defects in real time, ensuring only flawless products reach the market.
But how exactly do these systems work? What defects do they catch? And how do they help you stay compliant while boosting productivity?
Let’s dive deep.
An automatic tablet and capsule inspection machine is an advanced piece of equipment that uses high-speed cameras, sensors, and artificial intelligence (AI) to detect physical defects in tablets, softgels, and hard capsules.
It inspects for:
These systems run 24/7, often inspecting over 100,000 units per hour with up to 99.9% accuracy — far beyond what human inspectors can achieve.
Automatic inspection systems combine mechanical handling, imaging technology, and AI-powered decision-making.
Step-by-Step Process:
Manual inspection can miss defects due to fatigue, bias, or inconsistency. This is risky when even a single contaminated or broken tablet can:
Defects include:
Brahmi, Accura Pharmaquip’s flagship inspection system, uses:
It’s built for flexibility — whether you inspect tablets, softgels, or hard capsules, Brahmi adapts with minimal changeover time.
Yes. High-end systems like Brahmi are engineered to inspect multiple dosage forms using adjustable guides and programmable parameters.
You can switch between:
This versatility helps manufacturers reduce capital investment and floor space.
“What are the benefits of automatic inspection over manual?”
Here’s a breakdown:
| Feature | Manual Inspection | Automatic Inspection |
| Speed | 1,000–2,000 units/hour | 80,000–120,000 units/hour |
| Accuracy | ~80–85% | 99%+ |
| Consistency | Varies by operator | Uniform, algorithm-based |
| Compliance | Limited traceability | Full audit trail |
| Labor Cost | High | Lower long-term |
Automatic systems don’t just detect more defects — they also help document and improve your overall process with actionable insights.
“Is the inspection system GMP and FDA compliant?”
Yes. Any machine used in pharmaceutical production must meet cGMP, 21 CFR Part 11, and other global regulations.
Brahmi ensures:
This makes regulatory audits smoother and reduces non-compliance risks.
If you’re planning to upgrade your inspection process, evaluate these factors:
With decades of expertise in pharmaceutical automation, Accura Pharmaquip has designed Brahmi to deliver:
📢 Final Thoughts: Future-Proof Your Quality Control
As regulatory bodies get stricter and production scales grow larger, automated tablet and capsule inspection machines are no longer a luxury — they’re a necessity.
Investing in a system like Brahmi not only safeguards product quality but also positions your facility for long-term operational excellence.
📞 Want to schedule a demo or learn more about Accura’s Brahmi system?
Visit www.accurappl.com or contact our experts today.

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