Search Results for: Granulation Line

Due to the obvious advantages of direct powder compression, such as relatively simple process, no need for granulation and drying, fast product disintegration or dissolution, and stable product quality, about 40% of tablet varieties abroad have been produced by this process .   1 Application   ① Used for drugs that are easy to change […]

In recent years, the safety, stability and functionality of pharmaceutical excipients for oral solid dosage forms have received unprecedented attention. No matter the time, price is always our concern. But the most important thing besides considering the price factor is to ensure the quality of pharmaceutical excipients.   Therefore, taking lactose, cellulose derivatives, phosphate, and

Part 1 Introduction   With the development of science and technology, the intelligent manufacturing model is becoming a new hotspot and a new wind vane for technological competition and industrial protection in manufacturing. All walks of life in the world have carried out large-scale research, testing and exploration on intelligent manufacturing technology. Its production efficiency,

Changes in drug production sites may be related to changes in drug prescriptions, suppliers of raw and excipient materials, production processes, process parameters and batches, and other registration management matters, which is the most complicated of all change situations. This article discusses the technical risk considerations for the production site change of oral solid preparations

A generic drug is a drug that is consistent with the original drug (reference drug, RLD) in terms of dosage form, strength, route of administration, quality, curative effect, and use. Generics play a key role in the health care system, accounting for more than 50% of all prescriptions. Generic drugs are approved on the basis

Oral solid preparations of drugs are widely used clinically, and the attention paid to their quality and safety is lower than that of other dosage forms. The safety of oral solid preparations cannot be ignored. The 2010 version of drug GMP puts forward the concept of quality risk management. How to implement quality risk management

Oral solid preparation production plant layout has two-dimensional layout and three-dimensional layout, and there are various material conveying methods. Through case analysis, the application of gravity flow material conveying and automatic three-dimensional warehouse in three-dimensional plant layout is explained, and the three-dimensional layout and material conveying methods are summarized. Advantage.   Part 1 Overview  

Pharmaceutical water is widely used in the pharmaceutical production process and the preparation of pharmaceutical preparations, and is also used as a solvent, flushing agent, etc. The quality of pharmaceutical water directly affects the quality of medicines and is closely related to the safety of medicines. This paper summarizes and analyzes the management, quality control

Part 1 Tablet Overview   Tablets refer to medicinal material extracts, medicinal material extracts plus medicinal material fine powders into medicinal material fine powders and suitable excipients mixed and pressed in the form of discs or special-shaped tablets, including extract tablets, semi-extract tablets and whole powders piece. Tablets are solid drug-containing preparations made by compression

Benoate, also known as Painolate, Benluolai, and Jierean, its chemical name: 2-acetoxybenzoic acid p-acetylhelylphenyl ester, molecular formula: C17H15NO5, is a good non-steroidal Anti-inflammatory analgesics and cyclooxygenase inhibitors. Benoate tablet is a lipophilic compound synthesized by aspirin and paracetamol, which not only has significant analgesic, anti-inflammatory, and strong antipyretic effects, but also overcomes the disadvantages of