News
Patent-Backed Laser Drilling for Two-Chamber Os...
What goes wrong in osmotic tablet drilling, how CN2642449Y fixes it, and why HUANGHAI’s patented solution is a defensible, production-ready choice.
Patent-Backed Laser Drilling for Two-Chamber Os...
What goes wrong in osmotic tablet drilling, how CN2642449Y fixes it, and why HUANGHAI’s patented solution is a defensible, production-ready choice.
FDA 21 CFR Part 11 vs. EU Annex 11: How Pharma ...
FDA 21 CFR Part 11 and EU Annex 11 share the same spirit—data integrity—yet differ in emphasis and documentation. This guide compares the two and shows how HUANGHAI implements audit...
FDA 21 CFR Part 11 vs. EU Annex 11: How Pharma ...
FDA 21 CFR Part 11 and EU Annex 11 share the same spirit—data integrity—yet differ in emphasis and documentation. This guide compares the two and shows how HUANGHAI implements audit...
From Start-Up to Stable Output: On-Site Lessons...
Many teams experience the curve of “ramp-up → stabilize → optimize” after new equipment arrives. Based on two Shanghai pharma deployments, this article distills the steps that cut trial costs...
From Start-Up to Stable Output: On-Site Lessons...
Many teams experience the curve of “ramp-up → stabilize → optimize” after new equipment arrives. Based on two Shanghai pharma deployments, this article distills the steps that cut trial costs...
From URS to PQ: Laser Drilling Validation Path ...
From URS to PQ, laser drilling validation requires a complete Part 11-ready framework — including traceable records, audit trails, and integration with MES systems. HUANGHAI offers comprehensive documentation and training...
From URS to PQ: Laser Drilling Validation Path ...
From URS to PQ, laser drilling validation requires a complete Part 11-ready framework — including traceable records, audit trails, and integration with MES systems. HUANGHAI offers comprehensive documentation and training...
Can Pharmaceutical Testing Instruments Meet FDA...
Quality testing instruments—dissolution, disintegration, hardness, and friability—are central to regulatory submissions. Many markets now require traceable electronic records and permissions control. This article explains typical gaps, what Part 11 really...
Can Pharmaceutical Testing Instruments Meet FDA...
Quality testing instruments—dissolution, disintegration, hardness, and friability—are central to regulatory submissions. Many markets now require traceable electronic records and permissions control. This article explains typical gaps, what Part 11 really...
GMP Cleanliness & Dust Extraction: Hidden Essen...
Laser processing inevitably produces fine debris. Without engineered dust extraction and proper sealing, you risk poor hole quality, cross-contamination, and difficult cleaning validation. This article explains the pain points and...
GMP Cleanliness & Dust Extraction: Hidden Essen...
Laser processing inevitably produces fine debris. Without engineered dust extraction and proper sealing, you risk poor hole quality, cross-contamination, and difficult cleaning validation. This article explains the pain points and...