Quality

PIC/S Grade

API GMP and Materials control

Under API GMP principle, Hwang's ensure API's quality from the beginning, and double guarantee that API ,gets all of the requirement and is qualify to manufacture.

Process Validation

with fine effectiveness and reproducibility, we confirm that all of the process procedures are under the right condition.

Quality Verify

QC will inspect the complete quality of physical, chemical, and microorganism.

Discharge

Follow by testing from QC department, testing & manufacture control report, then the approval from QA manager which allow to transfer goods to warehouse.

GDP

GDP request documentation that can be trace back if certain investigation require. Make sure every shipment delivery are accurate and successful.

Quality Contro

How long and in which condition can medicine last? The acceleration stability test can be a main parameter to decide the shelf life of a product

Scope of Production

Specification of PIC / S GMP, divided into general preparation area, antibiotic ointment region, high sensitization Formulation Zone

Solid dosage forms

sugar-coated tablets (film-coated tablets, tablets, granules, powders) and capsules.

Semi-solid dosage form

ointment

Liquid dosage form

bismuth solution.

研發技術

專業研究開發團隊

研究開發人員經過相關文獻探討,評估技術可行性與相關法規,擬訂產品開發計劃,以科學技術及創新的思維理念,完成藥物的研究開發。

小型試製機

RD部門配有獨立多功能實驗機、旋轉式壓錠機、混合制粒機、真空乳化機、乾燥機...等先導型儀器設備,有效執行處方試驗。

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