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Process for directly compressing powder into tablets

Direct Powder Mixture Compression Process This process involves mixing drug powder with excipients and directly compressing the mixture into tablets

Tablet Quality Inspection Items and Packaging & Storage

I. Tablet quality inspection items mainly include appearance, weight variation, disintegration time, dissolution rate, content uniformity, and microbial limits. (1)

Common Forms of Pharmaceutical Packaging

Pharmaceutical packaging serves multiple functions, including protecting the medicine, facilitating use, and conveying information. It includes inner packaging, outer packaging,

Characteristics of Capsules

Definition and Characteristics of Capsules 1. Definition of Capsules Capsules are solid preparations made by filling pharmaceutical ingredients or excipients

Why are tablets coated, and what is the purpose of coating?

Coating is a key process in tablet production. This article focuses on the reasons and necessity for coating oral tablets.

Preparation process and optimization of solid dosage forms

Solid dosage forms play a crucial role in the pharmaceutical industry, and the process and performance of their manufacturing equipment

The Difference Between cGMP and GMP

1. What is cGMP?cGMP refers to current good manufacturing practices (GMP) regulations enforced by the FDA. cGMP provides a system

A Blister Card Stacking and Arrangement Device

Blister packaging machines are key equipment for automated pharmaceutical packaging, particularly for solid dosage forms such as capsules and tablets.

Solid Dosage Transport Validation

Solid Dosage transport validation is a crucial step in ensuring the stability of drug quality. It plays a vital role

Servo positioning system for automated adjustment of Blister Line’s format

The three units of the blister line are the blister unit, connection unit, and cartoning unit. Due to the current

China ranks second in the world in the number of new drugs under development

China ranks second in the world in the number of new drugs under development. Recently, it was learned from the

What does it mean for pharmaceutical equipment to follow GMP design?

GMP requirements for pharmaceutical Equipment can be divided into five key categories: · Equipment must not adversely affect product quality.