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发布时间: 2023 - 06 - 13
As one of the world's leading specialty chemical companies, Clariant contributes to value creation with innovative and sustainable solutions for customers from many industries.Our portfolio is designed to meet very specific needs with as much precision as possible. At the same time, our research and development is focused on addressing the key trends of our time. These include energy efficiency, renewable raw materials, emission-free mobility, and conserving finite resources. High performance excipients leveraged on high-quality standardsPharmaceutical Excipients for effective solubilization, bioavailability enhancement, controlled release, target delivery, stabilization, continuous manufacturing, preservation and viscosity enhancement.With a positive and progressive track-record ...
发布时间: 2023 - 06 - 13
A&C is a global GMP manufacturer of excipients, buffers, process solutions and a select number of active pharmaceutical ingredients (APIs). We have been servicing the life science industry since 1966, and expanded our footprint globally through the years. We currently have offices and GMP production facilities in North America and Europe.A&C works with a variety of products at our three GMP manufacturing facilities. We began with custom manufacturing of high purity solutions in 1966. The applications of our products include injectable, dermal, nasal, ophthalmic applications, preservatives, pH adjusters, cleaning solutions, solvents, flavours and aromatic compounds, lubricants, binders, antioxidants, process solutions and buffers. We offer GMP customized services for all our excipie...
发布时间: 2023 - 06 - 13
Antares Vitamin E TPGS has a record of safety based on decades of use in humans and animals and on reported toxicology studies. It is safe for transportation, storage and handling. Vitamin E TPGS has a self-affirmed GRAS (Generally Recognized As Safe) status when used as an oral dietary supplement of vitamin E.Antares Vitamin E TPGS solubilizes, emulsifies, and enhances the absorption of difficult to absorb lipophilic APIs in a wide range of pharmaceutical dosage forms and drug delivery systems. This ensures your drug will work as though it has high potency API.Advantages of Antares Vitamin E TPGS as an Emulsifying Agent in Pharmaceuticals:• Available in NF grade• Versatile, functional excipient with proven success in oral (solids and liquids), topical, ocular, mucosal and parent...
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BioSpectra
产品名称:

BioSpectra

上市日期: 2020-02-26

Country of Origin: USA

Tris - Trometamol,Injectable Grade

TRIS HCI 



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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