Content Uniformity: Tuân thủ giới hạn chấp nhận về đồng đều hàm lượng theo USP <905>/Ph. Eur.
Capsule Fill Weight: Trong dung sai khối lượng đóng nang mục tiêu ± theo kiểm soát trong quá trình
Disintegration Time: Tuân thủ giới hạn thời gian rã theo USP <701>/Ph. Eur.

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Laurus is expanding downstream into finished dosage forms (FDF) to add value beyond its cost-efficient, large-scale API operations. Its FDF development center brings together formulation and analytical research, clinical pharmacodynamics/pharmacokinetics, regulatory affairs, packaging development, IP management, and development QA. The company operates dedicated formulation labs, a lab-scale clinical supply facility, and analytical research labs able to develop a range of dosage forms. It is also building state-of-the-art oral FDF facilities meeting international regulatory standards, with a pilot plant and initial capacity of 1 billion units, planned to scale to 5 billion units, backed by roughly US$50 million in investment.