味の素コージンバイオ Product Lineup

Our company provides contract manufacturing of liquid media for customers in regenerative medicine, including iPS cells and mesenchymal stem cells. We perform aseptic filling into containers tailored to customer requirements. We can accommodate bottles and single-use bags. You can trust us to handle your needs with confidence. Please feel free to contact us with your requests. 【Factory Features】 ■ GMP-compliant manufacturing environment - Cleanliness, temperature and humidity, differential pressure management, environmental monitoring ■ Production line adapted for small quantities and diverse products - Extensive use of single-use equipment - Simple filling line - Smooth transition from research use to clinical use ■ Strict management of raw materials - Raw materials compliant with biological origin standards *Consultation for implementation audits is available. *For more details, please download the PDF or contact us.

We would like to introduce the "WFI Grade Water" that we handle. It is produced in a GMP-compliant manufacturing environment, so it can be used with confidence. Quality tests are conducted in accordance with the Japanese Pharmacopoeia, and a certificate of analysis is attached. Additionally, we can provide options such as bag capacity, tubes, and connectors to meet customer requests. 【Applicable Standards (Partial)】 ■Appearance: Colorless and clear liquid, with no odor ■TOC: Below 300 ppb ■Conductivity: Below 1.3 μS cm-1 ■Insoluble Matter: No easily detectable insoluble matter is recognized ■Sterility Test: Compliant *For more details, please download the PDF or feel free to contact us.

We provide contract manufacturing of buffers used in the manufacturing processes for biopharmaceuticals, vaccines, and cell therapies. We offer aseptic filling in containers tailored to our customers' requirements. 【Features】 ● GMP-compliant manufacturing environment Equipped with a video monitoring system in the manufacturing room Air conditioning and water facilities are monitored by an environmental monitoring system ● Strict raw material management Operated with a Manufacturing Execution System (MES) ● Adaptable to small quantities and a variety of products Introduction of single-use processes Stable and short delivery times ● Thorough quality control Analysis items are tailored to customer requests ● Stable procurement of materials Achieved stable procurement of materials through cooperation with domestic single-use manufacturers *Consultation available regarding implementation audits.

Ajinomoto Co., Inc. is working with domestic single-use product manufacturers to ensure stable procurement and achieve short delivery times. 【Requested Specifications】 ● 2D Single Use bag: 500mL, 1L, 2L, 10L, 20L ● 3D Single Use bag: 50L, 100L, 200L Customization is possible to match customer specifications, including tube length and connectors. We kindly ask you to consult with us. *If you wish to purchase single-use bags only, we will introduce you to a domestic single-use manufacturer contact.

We provide "WFI Grade Water" that complies with WFI standards in single-use bags. You can use it with confidence as it is produced in a GMP-compliant manufacturing environment, and we conduct quality tests according to the Japanese Pharmacopoeia, with test results attached. We can also accommodate your requests for bag capacity, tubes, connectors, and other specifications. 【Recommended for】 ■ Those who do not have production facilities for WFI grade water ■ Those who want to procure larger quantities of WFI grade water ■ Those who want to procure it more easily and at a lower cost than overseas products *For more details, please download the PDF or feel free to contact us.

We would like to introduce a case study of the implementation of "Custom Buffer" in the industry engaged in biopharmaceuticals, vaccines, and gene therapy. The customer faced challenges such as "having no space to prepare new preparation tanks" and "not having a manufacturing contractor due to the short time from composition confirmation to manufacturing." After the implementation, we were able to provide sterile products within three months of the customer's request and deliver products according to the customer's timing of use. [Case Overview (Partial)] ■Challenges - No space to prepare new preparation tanks - No manufacturing contractor due to the short time from composition confirmation to manufacturing - Desire to reduce the time for buffer preparation - Need for flexible response due to fluctuating usage quantities depending on the development items - No storage space, so we want the necessary quantities delivered at the desired timing *For more details, please refer to the related links or feel free to contact us.

We would like to introduce a case study of the implementation of "customer-specific original composition culture media" in the industry dealing with regenerative medicine. The customer faced challenges such as "lack of space to install new culture media preparation tanks" and "difficulty in managing the selection of raw materials due to the large number of materials used." After the implementation, we were able to provide the desired packaging according to the development stage and establish a stable supply system through collaboration with single-use bag manufacturers. 【Case Overview (Partial)】 ■Challenges - Lack of space to install new culture media preparation tanks - Difficulty in managing raw material selection due to the large number of materials used - Desire to reduce the time required for preparation work - Need for flexible supply due to fluctuations in usage depending on the development stage - No storage space available, wanting only the necessary amount at the required time *For more details, please refer to the related links or feel free to contact us.

In the pharmaceutical industry, particularly in the quality control department, the quality of the liquid media used for cell culture is a crucial factor that influences the safety and efficacy of products. Media manufactured in a GMP-compliant environment is essential to minimize the risk of contamination and ensure the reliability of test results. Our services provide sterile filling into containers tailored to customer requirements in a GMP-compliant manufacturing environment, supporting solutions to challenges in quality control. 【Usage Scenarios】 - Procurement of media in the cell culture process - Stabilization of media quality in the quality control department - Transition from research and development to clinical trials 【Benefits of Implementation】 - Quality assurance through GMP compliance - Increased efficiency in research and development due to stable supply - Cost reduction and shortened delivery times

In the pharmaceutical industry, the purity of the water used in manufacturing is extremely important to ensure the quality of pharmaceuticals. In particular, water that meets the standards for injection is essential for guaranteeing the safety and efficacy of products. Contamination with impurities can lead to a deterioration in product quality and pose health risks to patients. Our WFI-grade water is produced in a GMP-compliant manufacturing environment and has passed the quality tests of the Japanese Pharmacopoeia. This ensures that it meets high-quality standards in pharmaceutical manufacturing, allowing for safe use. 【Usage Scenarios】 - Preparation of culture media in pharmaceutical manufacturing - Preparation of buffers 【Benefits of Implementation】 - Improvement in pharmaceutical quality - Streamlining of manufacturing processes - Compliance with regulations

In the field of regenerative medicine, the purity of water is extremely important in cell culture and pharmaceutical manufacturing. In particular, high-purity water is essential for medium preparation, which affects cell survival rates and product quality. Contamination with impurities can lead to a decline in cell function and deterioration of product quality. Our WFI-grade water is produced in a GMP-compliant manufacturing environment and has passed the quality tests of the Japanese Pharmacopoeia. This ensures that it meets the high-quality standards required in regenerative medicine, allowing for safe use. 【Application Scenarios】 - Medium preparation in pharmaceutical manufacturing - Buffer preparation 【Benefits of Implementation】 - Improvement in pharmaceutical quality - Streamlining of manufacturing processes - Compliance with regulations

In the field of cell culture, the quality of the culture medium has a significant impact on cell proliferation and function. In particular, the purity of the water used in medium preparation is a crucial factor that affects cell survival rates and product quality. Contamination with impurities can lead to inhibited cell growth and degradation of product quality. Our WFI-grade water is produced in a GMP-compliant manufacturing environment and has passed the quality tests of the Japanese Pharmacopoeia. This ensures that high-quality standards are met in medium preparation, allowing for safe use. 【Application Scenarios】 - Medium preparation in pharmaceutical manufacturing - Buffer preparation 【Benefits of Implementation】 - Improvement in pharmaceutical quality - Streamlining of manufacturing processes - Compliance with regulations

In the biotechnology industry, a stable supply of liquid culture media optimal for cell culture is essential for product development. Particularly in the field of regenerative medicine, such as iPS cells and mesenchymal stem cells, the quality of the media affects the performance of the products. A GMP-compliant manufacturing environment and strict quality control are required. Our company offers contract manufacturing services for GMP-compliant liquid media to support your product development. 【Usage Scenarios】 - Cell culture in the field of regenerative medicine, such as iPS cells and mesenchymal stem cells - Development of biopharmaceuticals - Smooth transition from research media to clinical media 【Benefits of Implementation】 - Stable supply of high-quality media compliant with GMP - Aseptic filling into containers tailored to customer requirements - Reduction of research and development time and cost savings

In basic research at research institutions, it is important to have a stable supply of high-quality liquid culture media. In particular, the quality of the media significantly affects the experimental results when culturing iPS cells and mesenchymal stem cells. Liquid media manufactured in a GMP-compliant environment is essential for enhancing the reliability of research. Our company offers GMP-compliant liquid media contract manufacturing services, contributing to the improvement of research quality. 【Application Scenarios】 - Culturing iPS cells, mesenchymal stem cells, etc. - Research in the field of regenerative medicine - Cell culture experiments 【Benefits of Implementation】 - Improved experimental accuracy due to high-quality media - Stabilization of research plans through stable supply - Assurance of reliability through GMP compliance

In the regenerative medicine industry, particularly in scaffold fabrication, the survival and functional maintenance of cells are crucial. The appropriate selection of buffers is essential for optimizing the cellular environment and enhancing compatibility with scaffold materials. If the composition of the buffer is unstable or if manufacturing takes too long, it can lead to decreased efficiency in scaffold fabrication and potential delays in research and development or treatment. In our custom buffer implementation case, we provide buffers tailored to customer needs, supporting solutions to challenges in scaffold fabrication. 【Application Scenarios】 - Scaffold fabrication in regenerative medicine - Cell culture - Cell preservation 【Benefits of Implementation】 - Improved cell survival rates - Enhanced compatibility with scaffold materials - Increased efficiency in research and development

In the drug discovery industry, the quality and stability of buffers are crucial factors that influence the success of experiments during screening. Particularly, as the demand for increased efficiency and accuracy in screening grows, it is essential to shorten buffer preparation time, ensure uniform quality, and provide flexible responses. Our custom buffers address these challenges and contribute to the efficiency of screening. 【Use Cases】 - Screening experiments - Cell culture - Protein purification 【Benefits of Implementation】 - Reduction in buffer preparation time - Stable supply of high-quality buffers - Flexible responses tailored to experimental scale - Support for long-term stability testing

In the pharmaceutical industry, particularly in the quality control department, the quality of the liquid media used for cell culture is a crucial factor that influences the safety and efficacy of products. Media manufactured in a GMP-compliant environment minimizes the risk of contamination and enhances the reliability of test results. Our services provide high-quality liquid media through a GMP-compliant manufacturing environment and a stringent quality control system, supporting your quality management framework. 【Usage Scenarios】 - Procurement of media in the cell culture process - Ensuring media quality in the quality control department - Supply of media in the regenerative medicine field 【Benefits of Implementation】 - Quality assurance through GMP compliance - Increased efficiency in manufacturing processes due to stable supply - Reduction of contamination risks

1. Overview of Provided Content We provide broad support for custom media based on unique recipes, from research to commercial production. ◆ Types of Media: Original base media, Original feed media ◆ Process: Support from subculture to main culture ◆ Supply Formats: Bottles, various single-use bags (2D/3D) 2. Steps to Implementation We ensure a reliable implementation in 4 steps. (1) Prototype (Trial production at Engiran) (2) Culture Evaluation (Performance evaluation with actual cells) (3) Operational Design (Identifying issues and discussions) (4) Start of Main Supply (GMP-compliant system) 3. Supply and Logistics Scheme We have established a seamless network from raw material supply to product movement by coordinating our manufacturing base with external warehouses. We maintain thorough temperature control from room temperature to refrigerated and frozen conditions. 4. Benefits of Implementation ◆ Reduction of Labor Hours: Decrease in man-hours by outsourcing media preparation tasks ◆ Production Efficiency: Reduction of preparation errors and equipment maintenance risks ◆ Focus on Core Operations: Concentration of resources on core activities (drug discovery and process development)

In the vaccine manufacturing industry, there is a demand for streamlining the manufacturing process to ensure a stable supply of high-quality products. In particular, the quality of the culture media used for cell culture is a crucial factor that influences the efficacy and safety of vaccines. Mistakes in media preparation or variations in quality can lead to decreased manufacturing efficiency and quality issues with the products. Our liquid media is produced in a GMP-compliant manufacturing environment, providing stable quality to support the resolution of challenges in vaccine production. 【Usage Scenarios】 - Cell culture processes in vaccine manufacturing - Preparation processes for cell culture media - Stabilization of media quality 【Benefits of Implementation】 - Reduction of labor hours through outsourcing media preparation tasks - Decreased risk of preparation errors and equipment maintenance - Concentration of resources on core business (vaccine manufacturing)

In the field of regenerative medicine, the quality and safety of cells are the most important issues. The culture media used for cell culture must promote cell proliferation and provide a stable supply of high-quality cells. Our products are manufactured in compliance with GMP standards and strongly support cell culture in regenerative medicine. 【Application Scenarios】 - Cell therapy - Biopharmaceutical development - Research and development 【Benefits of Implementation】 - Stabilization of cell culture - Supply of high-quality cells - Increased efficiency in research and development

We have cataloged the "Sodium Hydroxide Solution" that we have received numerous requests for. This is a high-quality sodium hydroxide solution prepared with raw materials that meet the specifications of the three bureaus and WFI-grade water, produced in a GMP-compliant manufacturing environment. Quality tests are conducted in accordance with the Japanese Pharmacopoeia, and a certificate of analysis will be attached. Additionally, we can provide options such as bag capacity, tubes, and connectors to meet customer requirements. The packaging is designed for immediate use after delivery. 【Compliance Standards】 ■Appearance: In-house standards ■Conductivity: Reference value ■Neutralization Titration: 0.1mol/L: 0.09–0.11mol/L 0.5mol/L: 0.45–0.55mol/L 1.0mol/L: 0.9–1.1mol/L ■Filter Integrity: Compliant *For more details, please download the PDF or feel free to contact us.