20 YEARS OF PROFESSIONAL & DEDICATED SERVICE TO GLOBAL CUSTOMERS

Custom Manufacturing, Project Outsourcing, your Trusted Partner from China

The Manufacturing Process of Abarelix: Ensuring Purity and Efficacy

The production of synthetic peptides like Abarelix is a complex and highly regulated process, critical for ensuring the final product's purity, efficacy, and safety. As a synthetic decapeptide, Abarelix is typically synthesized using solid-phase peptide synthesis (SPPS) or solution-phase methods, followed by rigorous purification and lyophilization. The precise assembly of amino acids, including modified residues that enhance receptor affinity and resistance to degradation, is paramount. Each step in the manufacturing chain, from raw material sourcing to final product packaging, is subject to stringent quality control measures.

NINGBO INNO PHARMCHEM CO.,LTD. exemplifies the dedication to quality required in this field. Their operations are guided by international standards such as GMP and ISO 9001, ensuring that every batch of Abarelix powder meets the specified purity levels, typically exceeding 99%. The company's focus on abarelix synthesis and mechanism translation into a reliable product for various applications. This includes meticulous monitoring for potential impurities such as truncated sequences, oxidized forms, or deamidated peptides, which could compromise the drug's therapeutic performance or trigger adverse reactions. The drug formulation and stability of the lyophilized powder are also key considerations, ensuring a shelf life of up to two years when stored correctly at 2-8°C.

The application of Abarelix in treating advanced prostate cancer underscores the importance of robust peptide drug manufacturing. The ability to achieve consistent batch-to-batch quality is not just a regulatory requirement but a fundamental aspect of patient care. By understanding the detailed specifications and manufacturing processes, healthcare professionals and researchers can confidently utilize Abarelix in their critical work, supporting advancements in the field of hormone therapy and contributing to better patient outcomes in oncology.

Manufacturing Facilities

NINGBO INNO PHARMCHEM CO.,LTD. was established in 2007. It is committed to the R&D, production and sales of raw materials, pharmaceutical intermediates and fine chemicals. We striving to create a high-efficiency and high-quality integrated chemical service platform to better serve domestic and foreign customers.

Professional Export Experience

to Global Customers

WHY CHOSE US?

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).

FAQ

  • 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.

CONTACT US
Should you need to contact us; you may call during regular business hours, Monday through Friday, 8am – 6 pm.
NINGBO INNO PHARMCHEM CO.,LTD.
Address: No.163 Ruiqing Rd.,Ningbo 315000 China
Phone: 86-574-87319282
Fax: 86-574-27912196
SEND US AN EMAIL

NAME*

EMAIL*

COMPANY

COUNTRY*

MESSAGE*

Previous: Procuring High-Quality Abarelix: A Guide for Buyers

Next: Exploring GnRH Antagonist Therapeutic Uses Beyond Prostate Cancer

All Rights Reserved