Just like pharmaceutical cleanrooms, in tpbvsk cleanrooms are also popular lines that are characterized by 4 levels of cleanliness. This classification is based on the maximum number of sub-stools in the air. Join GMP Groups to learn about cleanroom lines and clean levels in BVSK food factory in the article below.

The investment process as well as the steps to implement a project in an industrial park include many quite complex procedures. GMP Groups will help investors understand general information about the process as well as procedures and points to note when investing in industrial parks.

Besides investing in industrial parks, investment outside the industrial park is also the type of interest to many investors. In the article below, GMP Groups will provide the process and way of investing projects outside the industrial park in the most detailed way.

Understanding the process for implementing an investment project not only helps the investor grasp the work to be done, but also ensures the legal conditions for the stable operation of the project. GMP Groups will provide you with information about the process of implementing two types of investment projects: investment projects in industrial parks and investment projects outside industrial parks. 

Medical equipment (TTBYT) is a special, essential item, present in every hospital and medical facility. In the context of the strong covid epidemic, businesses turned to manufacturing medical equipment partly to meet domestic supply, another part to be able to overcome difficult times during the epidemic. Accompanying businesses operating in medical equipment, GMP Groups sends customers the content of advice to announce the eligibility to produce medical equipment in the country.

GMP-WHO is a very familiar term, as well as a mandatory standard in the field of pharmaceutical manufacturing. So what is the GMP-WHO standard? What criteria does a pharmaceutical manufacturer that wants to meet the GMP-WHO standard have? Let’s find out with GMP Groups in the article below.

GMP-HS is a mandatory standard that any Health Protection Food Processing Unit (TPBVSK) needs to adhere to. What is the GMP-HS standard? What are the relevant standards? Join GMP Groups to learn more about these standards in the article below.

Good manufacturing practices (GMP) are one of the sets of principles and standards to be ensured for pharmaceutical production facilities. In the trend of global integration, Vietnamese production facilities not only need to meet domestic requirements but also comply with the requirements of other regions and territories such as GMP-EU, GMP-WHO, GMP-Japan standards. In this article, let’s find out what the GMP-EU standard is. How is GMP-EU different from GMP-WHO?

GMP Groups supports any organization to implement ISO 9001 or achieve ISO 9001 certification. We with years of experience in the field of Quality Consulting will provide you with guidance & professional know-how, coaching & mentoring, online and on-site training, samples and everything you need to achieve ISO 9001 Certification.

ISO 13485 is widely applied to medical device manufacturers. This is also a requirement if the manufacturing facility of medical instruments, medical devices, medical supplies wants its products to be widely recognized globally. The current version of ISO 13485 is ISO 13485:2016. What is ISO 13485? What are the benefits of applying ISO 13485 and which unit advises on prestigious standards? Join GMP Groups to find out in the following content.

According to Circular No. 36/2018/TT-BYT, in the drug manufacturing industry, drug production and storage facilities need to comply with GSP standards. So what is GSP? How do GSP standards and warehouses achieve GSP in the pharmaceutical industry? Which consultancy unit applies the GSP standard? Find out and contact GMP Groups as soon as you ask!

Any product before launching to the market must pass quality control and meet GLP standards. Let’s see what the GLP standard is with GMP Groups. What requirements do GLP-standard laboratories meet!

In addition to designing and constructing cleanrooms in key areas such as pharmaceuticals, cosmetics, food, veterinary and electronic, GMP Groups also provides an overall solution for cleanrooms in commonly applied fields such as:
Cleanrooms in the hospital sector
Cleanroom in the agricultural sector
Cleanroom in the field of research science

The cleanliness level used in electronic cleanrooms is classified according to ISO 14644-1:2015, the clean level gradually decreasing from ISO class 1 to ISO class 8. Join GMP Groups to learn about cleanroom lines and clean levels in the electronic component factory in the article below.

Depending on the nature of the product (sterile or non-sterile), the stages of production / treatment, environmental control requirements of the manufacturer that provide clean suitable for the veterinary cleanroom will be selected. Join GMP Groups to learn about cleanroom lines and clean levels in veterinary medicine factories in the article below.

The clean grade used in food processing depends on the nature of the product and the environmental control requirements from the manufacturer. Clean grade is classified under ISO 14644-1:2015. Join GMP Groups to learn about cleanroom lines and clean levels in the food factory in the article below.

In order to produce cosmetic products that meet the standards for the market, cosmetic factories use cleanroom systems as a mandatory and irreplaceable workspace. Join GMP Groups to learn about cosmetic production conditions, construction requirements and cleanroom lines of cosmetic factories in the article below.

In pharmaceutical cleanrooms, popular lines are characterized by 4 levels of cleanliness. This classification is based on the maximum number of sub-stools in the air. Join GMP Groups to learn about cleanroom lines and clean levels in pharmaceutical plants.

Among the many contractors designing cleanrooms on the market today, GMP Groups is a brand that many investors trust. The cleanroom design at GMP Groups consists of two main contents: Technology Section and System Section.

Cleanroom construction is one of the outstanding strengths of GMP Groups in the overall suite of cleanroom solutions that we provide. We provide a full range of construction items, bringing the highest benefit to customers.

In order to allow cleanrooms to be put into use and create products of the desired quality, meeting the requirements of relevant guidelines and laws, at each stage of the cleanroom, we must “Appraise and evaluate cleanrooms”. The evaluation and appraisal of clean rooms must always go hand in hand with the process of building a clean room. Find out about this service with the article below.

The GxP &ISO standard is a set of regulations and guidelines to solve the quality safety of products in a systematic and very effective way. Join GMP Groups to learn more about the GxP &ISO standard in the article below.

Currently in all areas, the use of measuring devices to monitor the control of process parameters is essential. This helps to achieve safe and quality end results. To ensure accurate measuring equipment, errors are within the permissible limits, these devices must first be manufactured by a quality, originating line system. Then those devices must be calibrated and inspected initially and periodically. 

Research on pharmaceutical preparation – cosmetics – food BVSK is the stage that is focused on the most professional investment in factories in this field. The article below will provide full information about GMP Groups’ product preparation research service.

Consulting production equipment, testing to suit the technology and investment rate as well as meeting GMP requirements during the appraisal process is a mandatory factor. In the following article, GMP Groups will introduce to readers the consulting service of production equipment and testing in accordance with GMP Groups’ GMP standards.