We manufacture treponemal antigens under the trade name of Yaohai. These are unique substances used to detect and diagnose some health problems. Before using an antigen for people, it must meet safety and performance requirements via a unique process called GMP manufacturing. This is an essential process, and in this article, we will discuss GMP manufacturing and why they are necessary for treponemal antigens.
GMP is short for Good Manufacturing Practice. This is a list of essential rules and regulations that companies like Yaohai PhD follow to ensure, everyone can benefit from their products in the most efficient and safe way. In the world of treponemal antigens, compliance with GMP means we ensure that our antigens are pure, safe and effective. This means that they are not mixed with aversive chemicals or contaminates, and work as it is intended to.
These guidelines help us to save money for the company and also to prevent any threats that will arise if the people using these antigens get suffered. The company uses GMP so they know what is in their products. The outcome of this can be happier customers who have more trust in the products they use. For patients needing these antigens, GMP is important to ensure the tests are accurate and reliable. Which means most local food animals can trust that the tests are working well, and if they need treatment.
Treponemal antigens require quite high quality [26]. Quality means that antigens are pure and functioning as they should. This is where guarded memory execution (GMP) comes in to save the day. Further, to make these antigens everything that we use needs to be methodically tested and checked according to GMP rules from material prep to tools used. These sorts of guidelines help us keep our products clean and at the highest quality possible. This also means that people may be sure that our treponemal antigens are safe and fully efficient,
These are not the only advantages of following GMP to prepare treponemal antigens but it would speed up and simplify the processes of making other treponemes. Companies can work on way, when they have set rules and materials and tools are the same every time. This allows them to make the antigens more rapidly and economically. This is critical for treponemal antigens because this will allow more people to be tested, and also in a shorter period of time. Basically, the faster we can produce these antigens, the more people will be able to benefit from them.
GMP Treponemal Antigen Manufacturing is a Top 10 biotech company specializing in microbiological fermentation. We have built a modern facility with strong RD capabilities and modern manufacturing facilities. Five production lines for pharmaceuticals in line with GMP standards for microbial purification and fermentation along with two automated fill and finish lines for vials and cartridges and pre-filled needles are available. The fermentation scales available are 100L, 500L, 1000L, to 2000L. Specifications for filling vials range from 1ml up to 25ml. the pre-filled syringes and cartridge filling specifications cover between 1-3ml. The workshop for production is cGMP compliant, and guarantees a stable supply of commercial products and clinical samples. Our factory produces large molecules that are shipped around the world.
GMP Treponemal Antigen Manufacturing is a Top 10 Microbial CDMO that incorporates quality control and regulatory matters. We have established a robust quality system that complies with the current GMP standards and regulations all over the world. Our regulatory team is well-versed on global regulatory frameworks to speed up biological launches. We guarantee traceable production processes and top-quality products that are compliant with the rules of US FDA, EU EMA, Australia TGA, and China NMPA. Yaohai BioPharma successfully passed an audit on site conducted by an accredited Qualified Person from the European Union (QP) to review our GMP system and production facility. Additionally, we've passed the first certification audits of the ISO9001 Quality Management System, ISO14001 Environmental Management System, and ISO45001 Occupational Health and Safety Management System.
Yaohai Bio-Pharma is a leading in microbial biologics CDMO. Our primary focus is the production of microbial vaccinations and therapeutics for managing pets, human and GMP Treponemal Antigen Manufacturing. We are equipped with cutting-edge RD platforms as well as manufacturing technologies that encompass the entire process beginning with the development of microbial strains and cell banking, to method and process development, to clinical and commercial manufacture that ensures the successful supply of new solutions. Through the years, we have accumulated vast knowledge of microbial-based bio processing. Over 200 projects have been successfully completed and we assist our clients to get through regulations, such as those of the US FDA and EU EMA. We also assist them in navigating Australia TGA and China NMPA. We are able respond promptly to market demands and offer tailored CDMO services thanks to our experience and expertise.
Yaohai Bio-Pharma is GMP Treponemal Antigen Manufacturing in microbial-derived biologics. We offer custom RD as well as manufacturing solutions, while minimising the risk. We've been involved in numerous modalities like recombinant subunit vaccines, peptides hormones, cytokines growth factors, single-domain antibodies, enzymes, plasmid DNA, the mRNA, and other. We are experts in several Microbial hosts, such as yeast extracellular and intracellular (yield up to 15 grams per liter) bacteria periplasmic secretion as well as soluble intracellular inclusion bodies (yield up to 10 grams/L). Additionally, we have developed the BSL-2 microbial fermentation platform for the development of bacterial vaccines. We have a track record of improving production processes, thereby increasing yields, and reducing costs. With a highly efficient technology team, we guarantee prompt and reliable project delivery and bring your products to market quicker.