Custom Manufacturing, Project Outsourcing, your Trusted Partner from China
At NINGBO INNO PHARMCHEM CO.,LTD., we are committed to delivering Pharmaceutical Grade Hydroxypropyl Methylcellulose (HPMC) that meets the highest standards of purity, safety, and efficacy. The pharmaceutical industry operates under stringent regulatory frameworks, and it is imperative that all excipients, including HPMC, comply with these rigorous guidelines. This article underscores the importance of these standards and how our Pharmaceutical Grade HPMC adheres to them.
The primary benchmarks for pharmaceutical excipients in major global markets are the United States Pharmacopeia (USP) and the European Pharmacopoeia (EP). These pharmacopoeias set detailed specifications for identity, purity, strength, and quality. For HPMC, compliance typically involves rigorous testing for parameters such as methoxyl and hydroxypropoxyl content, viscosity, residue on ignition, heavy metals, arsenic, lead, and microbial limits. Meeting these criteria ensures that the HPMC is free from harmful contaminants and will perform consistently and predictably in pharmaceutical formulations.
Our manufacturing processes for Pharmaceutical Grade HPMC are designed to guarantee compliance with USP and EP monographs. This involves meticulous quality control at every stage, from raw material sourcing to final product packaging. We employ advanced analytical techniques to verify that each batch meets all specified parameters. Furthermore, adherence to Good Manufacturing Practices (GMP) is fundamental to our operations, ensuring that HPMC is produced under controlled conditions that minimize the risk of contamination and assure product quality.
The importance of using compliant Pharmaceutical Grade HPMC cannot be overstated. It is the foundation upon which safe and effective medicines are built. By choosing HPMC from NINGBO INNO PHARMCHEM CO.,LTD., pharmaceutical manufacturers can be confident that they are utilizing an excipient that not only meets but often exceeds regulatory expectations. This commitment to purity and compliance is vital for safeguarding patient health and ensuring the successful development and commercialization of pharmaceutical products. Our dedication to quality means that our clients can focus on innovation, knowing their excipient supply chain is secure and reliable.
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.
