Strong sterilization ability: It can kill bacteria, fungi, viruses, spores and highly resistant bacterial spores (hydrogen peroxide fumigation can reach the level of LG6 sanitize, so that the number of microorganisms can be reduced by 6 logs, such as n*106→n, and the microbial killing rate is 99.9999%. )。

Do "space purification" and "space sterilization" mean the same thing to you? In the editor's view, they all play a role in sanitizing the space. If you think the same as the editor, then you are very wrong! In order to let you truly understand the meaning of "sterilization" and "purification", we have invited Marc Xiong, Executive Director of Biodeconta

Biodeconta is a dream that belongs to every Biodeconta person who wants to be able to provide truly efficient and high-quality microbial purification services, and to every Biodeconta who wants to have truly safe and intelligent microbial decontamination services

The biopharmaceutical zone of the Pharmaceutical Machinery Expo brings together many excellent biopharmaceutical equipment and service companies at home and abroad to display the latest technologies, products and solutions, and also becomes a window for industry professionals to have in-depth exchanges and explore the development direction and market trends of the biopharmaceutical industry. With an exhibition area of 10,000 square meters, the Biopharmaceutical Zone (Hall 2) of this year's Pharmaceutical Machinery Expo has gathered more than 100 professional exhibitors to systematically display the main process equipment and testing instruments for the production of drug substance and preparation, including solution preparation, bioreactor, separation, purification, filling, packaging and other equipment, biopharmaceutical consumables, analytical instruments and other inspection and testing instruments, as well as biopharmaceutical engineering design solutions and related services.

The purpose of revising Annex 1 is to reflect the changes that have occurred in the legislation and production of sterile medicinal products since the first edition in 2007. The latest revised version of EU GMP Annex 1 starts from the chapter on isolator systems, specifically proposing the integrity testing of gloves on isolator devices. The new regulations involve the definition of the time intervals for glove testing, thus standardizing the usage criteria for manufacturers. In fact, the first edition of Annex 1 drafted in 2007 stipulated that glove leakage tests must be carried out frequently, but did not provide any further specifications. The newly released revised version precisely fills this gap, stating that for isolators, glove tests must be conducted at specified time intervals, at least at the start and end of each production batch.

Anified laboratory biosafety standard is adopted. Pathogenic microorganisms are managed in a classified manner, and laboratories are managed in a graded manner.

Based on the infectivity of pathogenic microorganisms and the degree of harm to individuals and groups after infection, pathogenic microorganisms are classified into four categories. Among them, Category I and Category II are collectively referred to as highly pathogenic microorganisms, which can cause very serious/serious diseases in humans or animals. According to the biosafety protection level of laboratories, laboratories are divided into Level 1, Level 2, Level 3, and Level 4. Level 1 has the lowest protection level, and Level 4 has the highest protection level.

From November 17th to 19th, 2024, Biodeconta shone brightly at the China Pharmaceutical Equipment Exhibition.

At the exhibition site, the Biodeconta booth had a unique feature. The main color scheme of blue and white was bright, elegant, and in line with the characteristics of the pharmaceutical industry. The smooth layout design guided people to explore in depth.

In the fields of sterile pharmaceutical factories and pharmaceutical factory equipment, the GISTOOL - 100 Glove Leak Detector has always been highly favored for its outstanding performance and reliable quality. It is a powerful assistant in ensuring the aseptic production process, conducting precise detections to safeguard the quality of medicines.
Now, we are bringing you an unprecedented price offer! You can easily own this professional glove leak detector at a more affordable price.
Don't hesitate any longer. Seize this excellent opportunity to upgrade your pharmaceutical factory or pharmaceutical factory equipment. Choose the Biodeconta GISTOOL - 100 Glove Leak Detector and embark on a journey of efficient and precise detections.

Biodeconta Decontamination conducted regular hydrogen peroxide - based spatial cleaning, purification, and disinfection for the biological laboratory of a cell - therapy company in Beijing. This laboratory was established in accordance with GMP standards, and the client required the disinfection effect to reach the log6 level.

Laboratory animals are artificially bred animals with controlled microorganisms they carry, and have clear genetic backgrounds or known sources. They are used for scientific research, teaching, production, inspection, and other scientific experiments. They are classified into conventional (CV), specific pathogen free (SPF), and germ free (GF) grades.
The requirements for the environment of a laboratory animal facility are relatively strict. Besides environmental parameters such as temperature, humidity, and illuminance, there are also corresponding requirements for cleanliness and sedimentation bacteria. Taking an SPF laboratory animal facility as an example, the environment

The differences among "Cleaning", "Sanitizing", and "Disinfecting" are really easy to be confused. There are also significant distinctions in their Chinese translations. I believe that if "sterilizing" is added, a lot of people will probably feel dizzy. So, what on earth are the definitions of these words?