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
Introduce Sun Pharmaceutical Industries Ltd (Sun Pharma), a multinational pharmaceutical giant founded in 1983 by
In 2023 – the first year of the post-Covid era , the pharmaceutical industry experienced
On August 1, 2024, T&T Group and Ramky Group, a leading multinational corporation from India,
Drug recall involves the removal of pharmaceutical products from the market due to safety concerns
The “Vietnamese Drug Star Award” is a prestigious title the Ministry of Health awarded to
The Federal Trade Commission (FTC) is warning drug companies against improper patent filings, saying that
The 21st International Medical, Hospital, and Pharmaceutical Exhibition (Medi-Pharm Expo), which was held in Ho
EU GMP is a standard of good manufacturing practice for medicines issued by the European
With the introduction of the mARN vaccine against corona virus, Moderna earned a huge profit
1. General Introduction to Amvipharm – Global Healthcare Provider Amvipharm Joint Stock Company is a
1. General Introduction Fresenius Kabi is the market leader in Vietnam for infusion solutions and
1. Overview In 1997, the Nanogen Biopharmaceutical Technology Limited Liability Company was established with the
Pharbaco started out as an enterprise specializing in providing medicine to serve the army during
The relentless 16-year journey of Boston Vietnam, guided by the vision of “Research and improvement
With the ambition of becoming a leading generic drug manufacturer in Vietnam, HASAN – DERMAPHARM
The company currently holds 163 product registrations with the capacity to manufacture a diverse range
Overview Sanofi Aventis Vietnam Company Limited (Sanofi Vietnam) is a member of the Sanofi Group
Overview Korea United Pharm. Inc. – KUP, was founded in 1987 in Korea and has grown
The melting method represents a highly promising approach in the development of solid dispersions (SDs),
Differential Scanning Calorimetry (DSC) measures the heat released or absorbed by a sample as its
The shape of a tablet significantly affects compression, coating, blistering, and various physical-mechanical properties, as
Among the solvent evaporation methods for preparing solid dispersions, co-precipitation and supercritical fluid are two
Fluid-bed granulation (fluid-bed dryer) ) is a widely used solvent evaporation method in solid dispersion
The punch and die are two main parts in a tablet press, designed to perform
In bioequivalence studies (BE studies), reference drugs play a pivotal role in ensuring the accuracy
When a “blockbuster” drug’s patent expires, big pharmaceutical companies face intense competition from generic drug
The pervasive threat of N-nitrosamine impurities has emerged as a formidable challenge for the pharmaceutical industry,
Good Documentation Practices – GDP are essential pillars within the pharmaceutical industry, serving as the
In the context of globalization, the demand for high-quality pharmaceuticals is increasing, especially as new
Sterilization Process Sterilization is an important process used in the healthcare industry, pharmaceutical companies, and
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
In the previous post, SEN Pharma pointed out some limitations of paper batch records, which
What is the process validation? Process validation is the collection of data and documents that
A batch record is a mandatory GMP document in which every factor and action impacting
Even if the process is validated, the equipment is qualified, the in-process parameters are controlled,
Pharma Serialization – the process of assigning a unique identifier to pharmaceutical products to ensure
Ensuring the authenticity and integrity of medications throughout the supply chain remains a significant challenge
SUPAC (Scale-up and Post-approval Changes) is an important guidelines document that helps pharmaceutical manufacturers carry
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
In July 2022, the FDA published guideline providing recommendations for developing the content and format
On September 5th 2022, Mr. Do Xuan Tuyen, Deputy Minister of Health, promulgated the new
In pharmaceutical manufacturing, water plays a crucial role. Water can be a solvent in the
The environment is strictly controlled in pharmaceutical manufacturing plants to avoid microbiology and dust. Airlock
The drug liquid products have been one of the most popular dosage forms for centuries.
1. What is the Kaizen Method? Kaizen is a Japanese term that combines two words,
Increasing tablet output while ensuring pre-determined quality standards is the key task that drug makers
Origin of Organic Impurities Impurities are a crucial quality attribute of drug products because they
Principle When you shine a laser on an atom, the photon will excite the electron
In today’s fast-paced business environment, effective time management is a crucial skill for achieving success.
Time management is the art of organizing, allocating, and using time efficiently to achieve your
Feedback is essential for improving performance and quality of work. Effective feedback identifies strengths and
“Dealing” with negative feedback is an important skill for personal growth and maintaining healthy relationships.
