Aquigen Bio Launches Comprehensive Josamycin Propionate Impurity Standards Portfolio to Support Pharmaceutical R&D and Regulatory Compliance

Aquigen Bio, a leading global provider of pharmaceutical reference materials and impurity standards, proudly announces the launch of its Josamycin Propionate Impurity Standards category, reinforcing its commitment to supporting analytical precision and regulatory compliance in macrolide antibiotic research and production.
The newly introduced product line includes:

Josamycin Propionate
https://aquigenbio.com/product/josamycin-propionate/

Josamycin Propionate EP Impurity A
https://aquigenbio.com/product/josamycin-propionate-ep-impurity-a/

Josamycin Propionate EP Impurity B
https://aquigenbio.com/product/josamycin-propionate-ep-impurity-b/

These impurity standards are now available under the newly launched Josamycin Propionate category:
https://aquigenbio.com/products/impurity-standards/josamycin-propionate/

Why It Matters:
Josamycin Propionate is a critical macrolide antibiotic widely used in treating respiratory and soft tissue infections. As regulatory frameworks become increasingly stringent, pharmaceutical manufacturers are expected to quantify, qualify, and control impurities-especially those listed in pharmacopoeial monographs such as the EP (European Pharmacopoeia).
Aquigen Bio's meticulously synthesized and characterized impurity standards ensure:

High analytical accuracy for method development and validation

Seamless regulatory submissions

Enhanced confidence in impurity profiling and risk assessment
Empowering Precision in Drug Development and Quality Control
As global regulatory expectations rise, manufacturers and CROs (Contract Research Organizations) are under pressure to detect, quantify, and qualify even trace-level impurities. Impurities, whether process-related or degradation byproducts, can significantly affect drug safety, efficacy, and shelf life.

Aquigen Bio's new Josamycin Propionate impurity range has been developed with an unwavering focus on:
Analytical Integrity: Each product undergoes extensive QC using NMR, LC-MS, and HPLC techniques.

Global Regulatory Fit: Compliant with EP monographs and suitable for worldwide regulatory submissions.

Custom Documentation: Comprehensive CoA, Mass Spectra, Chromatograms, and ICH-compliant validation data.

Availability:
All Josamycin Propionate impurity standards are now available globally and come with detailed CoAs, NMR, LC-MS, and HPLC data, ready for immediate dispatch.

Aquigen Bio Sciences
281/1, Plot No 41,
Hinjawadi - Pirangut Rd,
Kasar Amboli, Pirangut,
Pune, Maharashtra 412108
Visit: www.aquigenbio.com

Aquigen Bio is a leading provider of certified reference standards, impurity profiling compounds, and research chemicals to pharma, biotech, and academic institutions worldwide. With a dedication to excellence and a focus on regulatory readiness, Aquigen empowers scientists to innovate with confidence.

This release was published on openPR.