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发布时间: 2025 - 09 - 29
DC Fine Chemicals, as a chemical supplier and manufacturer, knows how specific our sector is and we are committed to understanding the complexity of each of the companies we work with, whether they are large, medium or small.Through our involvement we aim to improve the specific needs of our partners, by helping them to avoid the need to add new suppliers and, therefore, a new unknown in the equation.By doing so, we optimise the process of buying research chemicals, allowing the R&D department to focus all its energy on what really matters, the development of our formulas that will lead to great products.
发布时间: 2025 - 09 - 29
Supplier, Manufacturer, Exporter of Fracturing Chemicals, IP BP USP Reagent FCC Food Grade Chemicals and Excipients, Muby Chemicals of Mubychem Group, established in 1976, is the original manufacturers of Specialty Chemicals, Pharmaceutical Excipient, Fragrance Food & Flavor chemicals, Reagent Grade Chemicals, Shale Gas Fracturing Chemicals in India. Mubychem Group has several manufacturing facilities spread across Western India and world wide contacts and toll manufacturers. We are exporting globally to countries like USA, Canada, Europe, UAE, South Africa, Tanzania, Kenya, Egypt, Nigeria, Cameroon, Uganda, Turkey, Mexico, Brazil, Chile, Argentina, Dubai, Korea, Vietnam, Thailand, Malaysia, Indonesia, Australia, China, Germany, France, Italy, Portugal, Bangladesh, etc.
发布时间: 2025 - 09 - 29
Anmol Chemicals Pharmaceutical Excipients, Food Grade Chemicals BP USP IP EP Ph Eur FCC Analytical Reagent ManufacturersAnmol Chemicals is a manufacturer supplier exporter of Pharmaceutical Excipients, Food Grade Chemicals and it offers materials as per IP BP EP Ph Eur USP NF JP FCC Food Grade as per the the latest monograph at best prices. Anmol Chemicals Group, established in 1976, is the pioneer manufacturer of Specialty Chemicals, Pharmaceutical Excipients, Some API, Food Chemicals in India. Anmol Chemicals Group has manufacturing facilities spread across Western India, representatives in Houston, Chicago USA and Dubai, UAE. We also have toll manufacturing units for processing chemicals in a few countries around the world. We make IP, BP, EP, USP, NF, Ph. Eur., JP, FCC or Foo...
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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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