고수율 인슐린 발효 공정 대한민국

• 당뇨병 치료사의 미래

  이것은 당뇨병에 대한 밝은 미래의 일각일 뿐이며 기술이 향상되고 새롭고 참신한 아이디어가 시장에 등장함에 따라 상황은 더욱 좋아질 것입니다. 이는 연구자들이 당뇨병을 치료하는 새로운 방법을 개발할 수 있는 잠재력을 가지고 있습니다. 이를 통해 당뇨병을 앓고 있는 사람들이 더 나은 삶을 영위할 수 있도록 돕고, 질병에 더 쉽게 대처하고 더 건강한 삶을 누릴 수 있습니다.

• 효율성 향상을 위한 인슐린 발효에 대한 혁신적인 접근 방식

  인슐린 합성의 새로운 발전 중에는 특정 박테리아와 관련된 흥미로운 발전이 있습니다. 이는 이러한 박테리아의 도움으로 이전보다 훨씬 빠르게 인슐린을 생산하는 데 도움이 됩니다. 이 접근법은 확실히 당뇨병 치료에 혁명을 일으킬 수 있습니다. 인슐린을 더 빨리 생산할수록 더 많은 사람들이 제때에 진정으로 필요한 치료를 받을 수 있습니다.

• 고수율 발효 공정

  그들은 또한 고수율 발효라고 알려진 새로운 기술을 가지고 있습니다. 이 과정을 통해 박테리아는 평소보다 더 많은 인슐린을 생산할 수 있습니다. 우리가 "설탕을 인슐린으로 전환시키는 박테리아"라고 부르는 것은 주변 환경이 좋아지면 인슐린 생산 수준을 증가시킬 수 있습니다. 우리는 한 번에 많은 양의 인슐린을 생산하기 때문에 모든 환자를 치료하려면 엄청난 양을 생산하는 것이 중요합니다. .

Yaohai 고수율 인슐린 발효 공정을 선택하는 이유는 무엇입니까?

• 강력한 공급망 및 제조 역량

  Yaohai Bio-Pharma, a top 10 High-Yield Insulin Fermentation Process of biological products, is a specialist in microbial fermentation. We have set up a modern facility that has robust RD capabilities and advanced infrastructure. Five lines of production for drugs conforming to GMP standards to purify and ferment microbial cells along with two fill and finish lines for vials as well as cartridges and needles pre-filled are readily available. The fermentation scales available for use range from 100L to 2000L. Filling specifications for vias are 1ml to 25ml, whereas pre-filled syringe or cartridge filling requirements are between 1-3ml. The production workshop is cGMP certified and offers the availability of commercial and clinical samples. The large molecules manufactured in our facility are available for delivery worldwide.

• 전문적 전문성과 폭넓은 경험

  Yaohai Bio-Pharma is a leading Microbial biologics CDMO. We have been focused on microbial-produced therapeutics and vaccines for human, veterinary, and the management of pet health. We are equipped with High-Yield Insulin Fermentation Process RD platforms as well as manufacturing technology that encompass the entire process beginning with the development of microbial strains cells, methods and processes, to commercial and clinical manufacturing which ensures successful implementation of cutting-edge solutions. We have acquired a large amount of experience in bio processing of microbial cells. We have delivered over 200 global projects, and help our clients with navigating the laws from the US FDA, EU EMA, Australia TGA, and China NMPA. Our professional expertise and extensive experience allows us to quickly respond to market demands and provide tailored CDMO services.

• 맞춤화, 효율성 및 비용 효율성

  Yaohai Bio-Pharma is experienced in biologicals derived from microbial sources. We provide customized RD solutions and manufacturing, while minimising potential risks. We have worked on various modalities, including recombinant subunit vaccines, peptides hormones, cytokines growth factors, single-domain antibodies enzymes, plasmid DNA various mRNAs, and more. We have specialized in multiple microorganisms, including High-Yield Insulin Fermentation Process intracellular and extracellular secretion (yields up to 15g/L) and intracellular soluble bacteria and inclusion body (yields up to 10g/L). We have also established a BSL-2 fermentation platform to create bacteria-based vaccines. We are experts in improving processes, boosting product yields, and decreasing production costs. We have a highly efficient technology team that ensures timely and top-quality project delivery. This allows us to bring your unique products faster to market.

• 품질 시스템 및 글로벌 규정 준수

  Yaohai BioPharma is a Top 10 Microbial CDMO that integrates quality management and regulatory affairs. We have a quality management system that is in compliance with current High-Yield Insulin Fermentation Process and regulations around the globe. Our regulatory team is knowledgeable in the global regulatory frameworks that help accelerate biological launches. We ensure traceable production procedures quality products, as well as in compliance with the guidelines of the US FDA and EU EMA. Australia TGA and China NMPA are also in compliance. Yaohai BioPharma has successfully passed the on-site audit by the European Union's qualified Person (QP) for our GMP quality system and production site. We also successfully cleared the first certification audits of the ISO9001 Quality Management System and ISO14001 Environmental Management System.

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