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API SUPPLIERS
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
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KDMF
Topscience Biotech specializes in R&D, production, sales of Sodium Hyaluronate, focusing on Cosmetics, Medical, Pharmaceutical Grade HA
Basic Nutrition, your expert for sourcing from China, India and Europe.
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
KDMF
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
KDMF
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
KDMF
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
KDMF
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USDMF
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Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
About the Company : Bioiberica is a global Life Science company with more than 45 years' experience in the production and development of molecules of high biological and therapeutic value for the phar...
Topscience Biotech specializes in R&D, production, sales of Sodium Hyaluronate, focusing on Cosmetics, Medical, Pharmaceutical Grade HA
About the Company : Established in 2005, Topscience located in Lanshan, Rizhao of PRC and covers an area of 100,000m². Products include Sodium Hyaluronate, Chondroitin Sulfate, Alpha-Arbutin, L-Ascor...
Basic Nutrition, your expert for sourcing from China, India and Europe.
About the Company : As an ISO9001, ISO22000 certificated supplier, Basic Nutrition supply high-quality ingredients for nutraceuticals. We can offer a range of products from small to large quantites: h...
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
About the Company : Established in 1994, Rochem is a distributor of pharmaceutical, food, nutritional and animal health ingredients to some of the largest companies in the world. It sources high-quali...
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API Imports and Exports
Drugs in Development
Lead Product(s) : Chondroitin Sulfate Sodium
Therapeutic Area : Musculoskeletal
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Bioiberica Rebrands Its Range of Nutraceutical Ingredients for Healthcare
Details : Bioiberica’s native (undenatured) type II collagen, Collavant® n2 (previously b2-Cool®) and the addition of Tendaxion® - a new brand for its tendon health ingredient.
Product Name : CSbioactive
Product Type : Other Small Molecule
Upfront Cash : Inapplicable
May 07, 2021
Lead Product(s) : Undenatured Type II Collagen,Chondroitin Sulfate Sodium,Hyaluronic Acid
Therapeutic Area : Musculoskeletal
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
New Study Further Validates Bioiberica’s B-2cool® Native Type II Collagen as Trusted Source for...
Details : The study, conducted in a rabbit model of osteoarthritis, set out to evaluate the effects of b-2Cool native type II collagen in combination with CS b-Bioactive chondroitin sulphate, glucosamine hydrochloride and Mobilee® which is a rooster comb extract ...
Product Name : Collavant n2
Product Type : Other Large Molecule
Upfront Cash : Inapplicable
July 09, 2020
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REF. STANDARDS & IMPURITIES
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PharmaCompass offers a list of Chondroitin Sulfate Sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Chondroitin Sulfate Sodium manufacturer or Chondroitin Sulfate Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chondroitin Sulfate Sodium manufacturer or Chondroitin Sulfate Sodium supplier.
PharmaCompass also assists you with knowing the Chondroitin Sulfate Sodium API Price utilized in the formulation of products. Chondroitin Sulfate Sodium API Price is not always fixed or binding as the Chondroitin Sulfate Sodium Price is obtained through a variety of data sources. The Chondroitin Sulfate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium Chondroitin Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Chondroitin Sulfate, including repackagers and relabelers. The FDA regulates Sodium Chondroitin Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Chondroitin Sulfate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Sodium Chondroitin Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Chondroitin Sulfate supplier is an individual or a company that provides Sodium Chondroitin Sulfate active pharmaceutical ingredient (API) or Sodium Chondroitin Sulfate finished formulations upon request. The Sodium Chondroitin Sulfate suppliers may include Sodium Chondroitin Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Chondroitin Sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium Chondroitin Sulfate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium Chondroitin Sulfate active pharmaceutical ingredient (API) in detail. Different forms of Sodium Chondroitin Sulfate DMFs exist exist since differing nations have different regulations, such as Sodium Chondroitin Sulfate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sodium Chondroitin Sulfate DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium Chondroitin Sulfate USDMF includes data on Sodium Chondroitin Sulfate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium Chondroitin Sulfate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sodium Chondroitin Sulfate suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Sodium Chondroitin Sulfate Drug Master File in Japan (Sodium Chondroitin Sulfate JDMF) empowers Sodium Chondroitin Sulfate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Sodium Chondroitin Sulfate JDMF during the approval evaluation for pharmaceutical products. At the time of Sodium Chondroitin Sulfate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Sodium Chondroitin Sulfate suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Sodium Chondroitin Sulfate Drug Master File in Korea (Sodium Chondroitin Sulfate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sodium Chondroitin Sulfate. The MFDS reviews the Sodium Chondroitin Sulfate KDMF as part of the drug registration process and uses the information provided in the Sodium Chondroitin Sulfate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sodium Chondroitin Sulfate KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Sodium Chondroitin Sulfate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sodium Chondroitin Sulfate suppliers with KDMF on PharmaCompass.
A Sodium Chondroitin Sulfate CEP of the European Pharmacopoeia monograph is often referred to as a Sodium Chondroitin Sulfate Certificate of Suitability (COS). The purpose of a Sodium Chondroitin Sulfate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sodium Chondroitin Sulfate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sodium Chondroitin Sulfate to their clients by showing that a Sodium Chondroitin Sulfate CEP has been issued for it. The manufacturer submits a Sodium Chondroitin Sulfate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sodium Chondroitin Sulfate CEP holder for the record. Additionally, the data presented in the Sodium Chondroitin Sulfate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sodium Chondroitin Sulfate DMF.
A Sodium Chondroitin Sulfate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sodium Chondroitin Sulfate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Sodium Chondroitin Sulfate suppliers with CEP (COS) on PharmaCompass.
A Sodium Chondroitin Sulfate written confirmation (Sodium Chondroitin Sulfate WC) is an official document issued by a regulatory agency to a Sodium Chondroitin Sulfate manufacturer, verifying that the manufacturing facility of a Sodium Chondroitin Sulfate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sodium Chondroitin Sulfate APIs or Sodium Chondroitin Sulfate finished pharmaceutical products to another nation, regulatory agencies frequently require a Sodium Chondroitin Sulfate WC (written confirmation) as part of the regulatory process.
click here to find a list of Sodium Chondroitin Sulfate suppliers with Written Confirmation (WC) on PharmaCompass.
Sodium Chondroitin Sulfate Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Sodium Chondroitin Sulfate GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Sodium Chondroitin Sulfate GMP manufacturer or Sodium Chondroitin Sulfate GMP API supplier for your needs.
A Sodium Chondroitin Sulfate CoA (Certificate of Analysis) is a formal document that attests to Sodium Chondroitin Sulfate's compliance with Sodium Chondroitin Sulfate specifications and serves as a tool for batch-level quality control.
Sodium Chondroitin Sulfate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Chondroitin Sulfate CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Sodium Chondroitin Sulfate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Chondroitin Sulfate EP), Sodium Chondroitin Sulfate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Chondroitin Sulfate USP).
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