Custom Manufacturing, Project Outsourcing, your Trusted Partner from China
Our commitment to quality begins with the sourcing of raw materials and extends through every stage of the Captopril synthesis process. We implement rigorous quality control measures, including advanced analytical techniques such as High-Performance Liquid Chromatography (HPLC), to verify the purity and identity of our Captopril intermediate. This ensures that the product consistently meets or exceeds the required >99% purity specification.
Certifications such as GMP (Good Manufacturing Practice), ISO 9001, and USP/BP standards are vital indicators of a supplier's adherence to international quality guidelines. These certifications demonstrate a commitment to producing intermediates that are safe for human consumption and suitable for pharmaceutical formulation. We proudly adhere to these benchmarks, providing our clients with the assurance they need.
The traceability of each batch is another cornerstone of our quality assurance. We maintain detailed records of production, testing, and distribution, allowing for complete transparency and accountability. This meticulous record-keeping is essential for regulatory compliance and for troubleshooting any potential issues that may arise during the drug development or manufacturing process.
When you partner with us for your Captopril intermediate needs, you are choosing a supplier that prioritizes quality at every level. Our dedication to producing a pharmaceutical-grade product ensures that your ACE inhibitor medications will be manufactured using the highest standards. This focus on quality is not just a regulatory requirement; it's a fundamental aspect of our mission to support global health through reliable pharmaceutical supply chains.
Investing in high-quality Captopril intermediate is an investment in the integrity of your finished products. We are dedicated to being a trusted source for pharmaceutical raw materials, providing the assurance that your Captopril supply will consistently meet the demanding standards of the pharmaceutical industry.
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.
