Custom Manufacturing, Project Outsourcing, your Trusted Partner from China
The pharmaceutical industry is one of the most heavily regulated sectors globally, with strict guidelines governing every stage of drug development and manufacturing. For pharmaceutical intermediates, adherence to these regulations is not just a requirement but a fundamental aspect of ensuring product safety and efficacy. NINGBO INNO PHARMCHEM CO.,LTD. places paramount importance on regulatory compliance for all its products, including vital Ticagrelor intermediates.
When pharmaceutical companies seek to buy Ticagrelor intermediate online, they must ensure that their suppliers meet stringent quality and regulatory standards. This includes certifications such as GMP (Good Manufacturing Practice) and ISO standards. NINGBO INNO PHARMCHEM CO.,LTD. proudly holds these certifications, demonstrating our unwavering commitment to producing intermediates that are safe, pure, and consistently manufactured according to international benchmarks.
The purity and traceable origin of intermediates like Ticagrelor Intermediate (CAS 274693-27-5) are crucial for the final API. Regulatory bodies require detailed documentation, including Certificates of Analysis (CoA) and Material Safety Data Sheets (MSDS), which NINGBO INNO PHARMCHEM CO.,LTD. readily provides. Our role as a dependable provider of pharmaceutical intermediates for cardiovascular drugs extends to ensuring full transparency and documentation for our clients.
Navigating the complex regulatory landscape requires specialized knowledge and a proactive approach. NINGBO INNO PHARMCHEM CO.,LTD. maintains a dedicated team that stays abreast of the latest regulatory requirements in major global markets. This ensures that our clients receive intermediates that comply with all necessary standards, facilitating smoother drug approvals and market access.
As a trusted source for the Ticagrelor synthesis raw material and other chemical building blocks, NINGBO INNO PHARMCHEM CO.,LTD. understands that regulatory compliance is the bedrock of pharmaceutical manufacturing. We are committed to supporting our clients by providing compliant, high-quality intermediates that contribute to the development of safe and effective medicines.
Manufacturing Facilities
Professional Export Experience
to Global Customers
1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;
2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;
3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).
A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.
A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.
A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.
