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发布时间: 2025 - 08 - 04
Founded in 1916 as Tetralin GmbH, we look back on over 100 years of company history. In 1931, Deutsche Hydrierwerke (DHW) in Rodleben patented and implemented the world's first industrial production plant for fatty alcohols using catalytic high-pressure hydrogenation. This significant development in oleochemistry laid the foundation for the production of high-performance detergents and care products. Deutsche Hydrierwerke's experience in catalytic hydrogenation reactions in the production of fatty and sugar alcohols enabled the development of esters and ethers, sugar derivatives, and other chemical specialties. In 1991, DHW GmbH Rodleben was integrated into the globally active oleochemical group of the Indonesian company Salim. With the formation of Ecogreen Oleochemicals in 2001, ...
发布时间: 2025 - 08 - 04
Born in Valenza Pò (Alessandria) in 1946, the company later moved to Borgoricco, a town 15 km from Padua and 25 km from Venice in northeastern Italy.I.C.V. established itself as a market leader since its founding. In 1984, it became part of the Bertolino Group, a family-run group, a leading producer of ethanol and other wine-related products, combining its diverse experience in the sector with sophisticated production facilities and advanced technologies.Thanks to the vision and tenacity of Antonina Bertolino, president of the I.C.V. board of directors, the company underwent a complete restructuring and successfully increased production capacity and improved process efficiency, while fully respecting the environment.
发布时间: 2025 - 08 - 04
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BioSpectra
产品名称:

BioSpectra

上市日期: 2020-02-26

Country of Origin: USA

Tris - Trometamol

UREA 

Potassium Bromide

BioSpectra


Company Profile


BioSpectra is a US Based manufacturer of GMP, pharmaceutical grade ingredients, including Actives, Excipients, GMP Process Chemicals & Bulk GMP Buffers and Solutions. Our focus is small molecule synthesis and true, phase change multistep purification for both traditional and bio-pharmaceutical applications.  Our services include Contract GMP product development coupled with ongoing commercial manufacturing and regulatory support up to and including DMF submissions.  All our manufacturing processes are fully validated.  Our US-GMP regulatory package complies with IPEC & ICHQ7 guidelines. Our onsite analytical testing capabilities include multi-compendial and custom specifications with full traceability and transparency of all raw materials and sources. Our commitment is to quality, compliance and true, US-GMP manufacturing, testing and regulatory support is unparalleled.  We own and operate out of 175,000 square feet of FDA registered & inspected GMP manufacturing space, operating under the most rigorous quality system while holding to the most stringent regulatory demands. Our goal is to be a valued partner in the secure supply chain and the solution to any key ingredient issue our customers may have.



PREMIUM PHARMACEUTICAL INGREDIENTS - MANUFACTURED EXCLUSIVELY IN THE USA


GMP Product Categories

• Active Substances

• GMP Custom Products

• Excipients and Key Ingredients

• GMP Process Chemicals and Solutions

• Bulk, GMP Biological Buffers & Denaturants


Custom GMP Products

• Purification of Key Ingredients

• Full GMP Product Development

• Small Molecule Custom Synthesis

• API Development & Manufacturing

• GMP Compounded Solvents & Solutions


Comprehensive Quality and Regulatory Program

• FDA Registered and Inspected

• Document Support - DMF Submissions

• FDA & ICH Q7 Guidance for Drug Substances

• Global GMP Requirements – US, IPEC, ICH Q7

• State-of-the-art Instrumentation & Laboratories


Corporate Values & Commitments

• True GMP Product Claim – Always Synthesized and/or Purified not simply tested and repackaged

• Reliable, Consistent, Uniform, Quality-Based Manufacturing of Premium Pharmaceutical Ingredients

• Authentic, Secure Supply Chain - 100% Traceable Raw Materials from Qualified Sources

• Fully Validated GMP Manufacturing Systems & Qualified Equipment

• Exclusively Manufactured in the USA


Comprehensive Quality & Regulatory System

• FDA Registered & Inspected

• Full Transparency in Documentation

• Stringent Quality Program & Controls

• Document Support – DMF Submissions

• Rigorous compliance to Global Standards

• FDA & ICH Q7 Guidance for Drug Substances

• Global GMP Requirements – US, IPEC, ICH Q7

• State-of-the-art Instrumentation & Laboratories

• Culture of Embracing Evolving Regulatory Demands

• Complete Testing of all Raw Material and Finished Products


BioSpectra offers four different grades of its materials from two manufacturing sites in Pennsylvania. Each grade of material is manufactured to meet specific end-use needs.


Bio Active Grade products are manufactured in our Bangor, PA facility, which is registered and inspected by the Federal Food and Drug Administration, in accordance with ICH Q7 guidelines incorporating qualified equipment and utilities, validated processes and fully traceable supply chains. Type II Drug Master Files may be referenced through a supply agreement.


Bio Excipient Grade products manufactured in accordance with ICH Q7 guidelines and Bio Pharma Grade products manufactured in accordance with IPEC guidelines are produced in our Bangor, PA and Stroudsburg, PA facilities.


Bio Active LBLE Grade products are intended for use in sterile applications. These products are manufactured in our Bangor, PA facility, which is registered and inspected by the Federal Food and Drug Administration, in accordance with ICH Q7 guidelines incorporating qualified equipment and utilities, validated processes and fully traceable supply chains. Type II Drug Master Files may be referenced through a supply agreement.


For more information, please visit: https://www.biospectra.us/technical/manufacturing-capabilities

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