EU GMP is a standard of good manufacturing practice for medicines issued by the European Medicines Agency (EMA), covering all principles and standards to control activities or problems occurring in pharmaceutical manufacturing facilities in order to ensure the safety, efficacy, stability, and uniformity of each batch of products. Advantages of
The 21st International Medical, Hospital, and Pharmaceutical Exhibition (Medi-Pharm Expo), which was held in Ho
With the introduction of the mARN vaccine against corona virus, Moderna earned a huge profit
Did you know that cancer is the major cause of death, disability, and medical burden
Believe it or not, there are 2 separate big names in the pharmaceutical industry which
At the Government’s regular press in September, Ms. Nguyen Thi Mi Huong, Deputy Minister of
On September 8th, Mr. Do Xuan Tuyen – Deputy Minister of Health – said “More
1. What is the Kaizen Method? Kaizen is a Japanese term that combines two words,
Nowadays, the pharmaceutical industry’s term M&A (Mergers and Acquisitions) is no longer unfamiliar to readers.
As we already know, Singapore is famous for being a global financial center. Recently, this
1. Chemical structure Pregelatinized starch is partially or fully modified starch by chemical and mechanical reactions. The
1. Chemical structure Croscarmellose sodium (CCS) is a cross-linked polymer of carboxymethyl cellulose sodium. 2.
1. Chemical structure Crospovidone is a cross-linked polymer of PVP, insoluble in water. 2. Pharmacopoeia
1. Chemical structure Carboxymethylcellulose Calcium is a salt of calcium with the polycarboxymethyl ether of
Empagliflozin is an SGLT2 inhibitor currently used to treat type 2 diabetes under the brand
1. Overview [1]–[3] Apixaban is a new class of anticoagulant that blocks the clots forming
Co-processed excipients are mixtures of different excipients that are physically treated to change their physical
EU GMP is a standard of good manufacturing practice for medicines issued by the European
In 2022, many pharmaceutical factories were entangled in data integrity (DI) issues during inspections by
Medicine is of significance for human well-being, thus, the pharmaceutical production process must adhere strictly
The Federal Trade Commission (FTC) is warning drug companies against improper patent filings, saying that
This circular prescribes marketing authorization registration of contract manufactured medicine, medicine of technology transfer in
On November 29, 2022, the Medicines and Healthcare Products Regulatory Agency (MHRA) announced new serious
Not all products go through FDA experts’ evaluation before they are offered for sale. In
The environment is strictly controlled in pharmaceutical manufacturing plants to avoid microbiology and dust. Airlock
In the previous post, SEN Pharma pointed out some limitations of paper batch records, which
The drug liquid products have been one of the most popular dosage forms for centuries.
A batch record is a mandatory GMP document in which every factor and action impacting
Increasing tablet output while ensuring pre-determined quality standards is the key task that drug makers
What do we know about N-nitroso compounds (NOCs)? NOCs were first discovered about 40 years
Principle When you shine a laser on an atom, the photon will excite the electron
