Custom Manufacturing, Project Outsourcing, your Trusted Partner from China
For pharmaceutical manufacturers, procuring intermediates that adhere to current Good Manufacturing Practices (cGMP) is not optional; it's a regulatory imperative and a cornerstone of product quality. NINGBO INNO PHARMCHEM CO.,LTD. exemplifies this commitment through its production and supply of 1-(4-aminophenyl)-5,6-dihydro-3-(4-morpholinyl)-2(1H)-pyridinone (CAS: 1267610-26-3), a crucial Apixaban intermediate.
Our manufacturing facilities operate under strict quality management systems, ensuring that every batch of this high purity pharmaceutical intermediate 1267610-26-3 meets the most demanding cGMP standards. This rigorous control is essential for compounds like this, which directly impact the safety and efficacy of the final Apixaban drug product. As a dedicated 1-(4-aminophenyl)-5,6-dihydro-3-(4-morpholinyl)-2(1H)-pyridinone manufacturer, we understand these responsibilities deeply.
The procurement of cGMP-compliant intermediates requires thorough due diligence. Pharmaceutical companies need to verify not just the product's specifications but also the supplier's adherence to regulatory guidelines. NINGBO INNO PHARMCHEM CO.,LTD. provides comprehensive documentation and transparent processes, making it easier for our clients to meet their own compliance obligations when they buy 1-(4-aminophenyl)-5,6-dihydro-3-(4-morpholinyl)-2(1H)-pyridinone.
Furthermore, we strive to offer a competitive 1-(4-aminophenyl)-5,6-dihydro-3-(4-morpholinyl)-2(1H)-pyridinone price, recognizing the economic pressures within the pharmaceutical industry. Our ability to provide a high-quality Apixaban synthesis precursor at a favorable cost positions us as a preferred pharmaceutical intermediate supplier for companies globally.
In essence, partnering with NINGBO INNO PHARMCHEM CO.,LTD. for your 1-(4-aminophenyl)-5,6-dihydro-3-(4-morpholinyl)-2(1H)-pyridinone needs means securing a product that is not only chemically excellent but also manufactured under conditions that fully support your cGMP requirements. This commitment to quality and compliance underpins our contribution to the global pharmaceutical supply chain, ensuring safe and effective medications reach patients.
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.
