Our company has received notification from the patent office that the patent certificate for "Composition for Upper Respiratory Tract Drug Delivery and Its Administration Method" has been granted in China, with application number 202211335382.4.
Our company has signed a contract with Company S, which focuses on the cross-strait medical aesthetics market. Through our nano-emulsion technology, we will assist Company S in developing a sustained-release vitamin C+E product. Subsequently, Original BioMedical will exclusively supply the core raw materials.
Original BioMedicals is a specialized technology platform company for innovative drug development and pharmaceutical development services, possessing strong research capabilities and a wealth of product resources. Xinbai Pharmaceutical is a subsidiary of China Resources Pharmaceutical Group, while Rongchang Pharmaceutical is a professional pharmaceutical distributor. Adhering to the principles of win-win cooperation and joint development, the three parties will leverage their respective strengt
Our company has obtained an Australian invention patent for the "Composition for Upper Respiratory Tract Drug Delivery and Its Administration Method," with certificate number 2022259787.
Our company has obtained a Japanese invention patent for "Composition for Upper Respiratory Tract Drug Delivery and Its Administration Method," with certificate number Patent No. 7514898.
Extends drug half-life
Reduce the side effects of drug
Nanocomposite microcells + Metal controlled release
Scale-up and commercialization of the manufacturing process
High drug stability
Design of the particle size
I ron chelators and iron can be used together to regulate drug release time
Improved new drugs
Clinical shortcomings of modified drugs
Fast forensics / High success rate
Functional excipients
We specialize in the development of new drugs without new ingredients, focusing on new formulations, new dosages, and new indications in drug delivery systems to enhance efficacy and reduce side effects. By repurposing existing drugs, we shorten development time and save drugs that are at risk of failure. Our research and development process includes synthesis, purification, method development, formulation design, and safety testing. Clinical production is completed by cGMP-certified manufacturing facilities.
