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From “Accurate” to “Reliable”: Engineering Esse...
As regulations tighten, inspection and rejection determine whether drilling quality is provable and traceable. A vision system isn’t just “taking pictures”—it must be tightly coupled with line takt, rejection actuators,...
From “Accurate” to “Reliable”: Engineering Esse...
As regulations tighten, inspection and rejection determine whether drilling quality is provable and traceable. A vision system isn’t just “taking pictures”—it must be tightly coupled with line takt, rejection actuators,...
How ODF Coating Lines Meet FDA 21 CFR Part 11 C...
As ODF dosage forms expand globally, regulatory compliance has become a key evaluation criterion for pharmaceutical manufacturers.HUANGHAI’s MJ150 and MJ150-L ODF coating systems are designed with full FDA 21 CFR...
How ODF Coating Lines Meet FDA 21 CFR Part 11 C...
As ODF dosage forms expand globally, regulatory compliance has become a key evaluation criterion for pharmaceutical manufacturers.HUANGHAI’s MJ150 and MJ150-L ODF coating systems are designed with full FDA 21 CFR...
How Our Laser Drilling System Supports FDA 21 C...
For controlled-release osmotic tablets, consistent laser drilling isn’t enough — compliance is equally critical.The HUANGHAI Olando K3-2 Laser Drilling System integrates FDA 21 CFR Part 11-ready features such as user...
How Our Laser Drilling System Supports FDA 21 C...
For controlled-release osmotic tablets, consistent laser drilling isn’t enough — compliance is equally critical.The HUANGHAI Olando K3-2 Laser Drilling System integrates FDA 21 CFR Part 11-ready features such as user...
Olando K3-2 vs Other Brands: The Practical Choi...
Side-by-side comparison for procurement & engineering teams: operation, cleaning, throughput, compliance, and service response.
Olando K3-2 vs Other Brands: The Practical Choi...
Side-by-side comparison for procurement & engineering teams: operation, cleaning, throughput, compliance, and service response.
What Is FDA 21 CFR Part 11 and Why It Matters f...
FDA 21 CFR Part 11 defines how electronic records and signatures must be managed to ensure data integrity, traceability, and authenticity in pharmaceutical production. HUANGHAI integrates Part 11 features—user access...
What Is FDA 21 CFR Part 11 and Why It Matters f...
FDA 21 CFR Part 11 defines how electronic records and signatures must be managed to ensure data integrity, traceability, and authenticity in pharmaceutical production. HUANGHAI integrates Part 11 features—user access...
Inline vs Offline: How to Choose the Right Prod...
Inline reduces WIP and handling by syncing equipment along the line; offline adds flexibility for multi-SKU operations but introduces transfer and data stitching. This article provides a practical decision matrix—throughput,...
Inline vs Offline: How to Choose the Right Prod...
Inline reduces WIP and handling by syncing equipment along the line; offline adds flexibility for multi-SKU operations but introduces transfer and data stitching. This article provides a practical decision matrix—throughput,...