News
Decoding FDA 21 CFR Part 11 and EU Annex 11: Wh...
FDA 21 CFR Part 11 and EU Annex 11 define how electronic records and signatures must be controlled in pharma. This article compares the two regulations, explains HUANGHAI’s dual-compliance design...
Decoding FDA 21 CFR Part 11 and EU Annex 11: Wh...
FDA 21 CFR Part 11 and EU Annex 11 define how electronic records and signatures must be controlled in pharma. This article compares the two regulations, explains HUANGHAI’s dual-compliance design...
Why IQ/OQ/PQ and cGMP Validation Matter for Pha...
IQ/OQ/PQ and cGMP are more than buzzwords in pharma equipment projects. They define how a line is installed, tested and proven under real production conditions. This article explains the basics...
Why IQ/OQ/PQ and cGMP Validation Matter for Pha...
IQ/OQ/PQ and cGMP are more than buzzwords in pharma equipment projects. They define how a line is installed, tested and proven under real production conditions. This article explains the basics...
From Formulation to Commercial Scale: Co-Develo...
Advanced equipment alone cannot guarantee ODF success. HUANGHAI’s co-development model integrates formulation, process and equipment — from early recipe design and pilot trials to parameter matching, validation documents and flexible...
From Formulation to Commercial Scale: Co-Develo...
Advanced equipment alone cannot guarantee ODF success. HUANGHAI’s co-development model integrates formulation, process and equipment — from early recipe design and pilot trials to parameter matching, validation documents and flexible...
Continuous or Traditional? Building an Efficien...
Traditional ODF manufacturing often uses stand-alone machines and experience-based scale-up, which can struggle with complex films and high validation costs. This article compares traditional and integrated continuous models, and explains...
Continuous or Traditional? Building an Efficien...
Traditional ODF manufacturing often uses stand-alone machines and experience-based scale-up, which can struggle with complex films and high validation costs. This article compares traditional and integrated continuous models, and explains...
Unified Tablet Testing Logbook: From Weight to ...
Many QC labs still track tablet weight, hardness, friability and disintegration in separate files. This article shows how to design a unified tablet physical testing logbook—and how HUANGHAI instruments like...
Unified Tablet Testing Logbook: From Weight to ...
Many QC labs still track tablet weight, hardness, friability and disintegration in separate files. This article shows how to design a unified tablet physical testing logbook—and how HUANGHAI instruments like...
From Weight to Friability: Building a Unified T...
A practical guide to unifying tablet weight, hardness, friability, thickness and disintegration results into one physical testing logbook—so QC labs can see trends, speed audits, and link tests back to...
From Weight to Friability: Building a Unified T...
A practical guide to unifying tablet weight, hardness, friability, thickness and disintegration results into one physical testing logbook—so QC labs can see trends, speed audits, and link tests back to...