GMP API grade material | Ph EUR compliant | Supply according to GDP | Trusted European API Partner

CDCA / Chenodeoxycholic Acid Buying Guide 2024

Buying a high-quality GMP-grade Active Pharmaceutical Ingredient (API) like chenodeoxycholic acid (CDCA) online comes with some challenges at first, such as quality issues, shipping procedures, payment options, compliance requirements, and more. MedicaPharma offers you premium-grade Chenodeoxycholic acid (CDCA) that is produced in Europe.

All our active pharmaceutical ingredients (APIs) are manufactured according to high GMP standards, mainly according to the European Pharmacopeia.

We Serve Leading Global Healthcare and Research Organizations

MedicaPharma is a trusted partner for a range of businesses across multiple sectors in the healthcare industry.


Commercial Businesses

biotechnology trends

Research Companies


Educational Institutions

CDCA Buying Process

There are many options available when purchasing CDCA online. Here are four steps to guide the process: 

Step 1: Identify Your CDCA Requirements

CDCA is available in different forms, purity, and strengths. While CDCA has a constant molecular structure, it can be found in various forms or preparations depending on factors such as purity, formulation, and delivery method. 

Some variations to consider when purchasing CDCA include: 

Purity and Formulation

GMP-grade APIs like CDCA used for medical or research purposes are often produced in a highly purified form. The purity level is crucial, especially when CDCA is intended for pharmaceutical use or clinical studies. Choose a manufacturer that provides CDCA with your specified purity levels and formulation requirements. 

Pharmaceutical Grade 

Pharmaceutical-grade CDCA must meet strict GMP quality standards to ensure suitability for medical applications. This grade of CDCA is often used to develop medications and treatments for conditions such as gallstones and liver disorders.

Research Grade

Research grade CDCA is used in laboratory or experimental settings for research purposes. This form is typically suitable for studies investigating the mechanisms of CDCA in various processes for different fields such as healthcare and biotechnology.

Delivery Forms

Research institutions, hospitals, and commercial enterprises typically buy GMP-grade APIs like CDCA in different forms, such as capsules or tablets. This allows for convenient administration in clinical settings or for individuals undergoing treatment. The choice of formulation depends on the specific treatment requirements or research.


In clinical research, CDCA might be used in microencapsulated form. This involves enclosing small particles of CDCA within protective capsules. Studies related to diabetes treatment may use this form to protect and transport islets –  cells located in the pancreas that maintain blood sugar levels.

Combination Formulations

CDCA is sometimes formulated in combination with other medications or substances. For example, it might be part of a medication designed to address multiple aspects of liver function or digestive health.

When purchasing CDCA, it’s essential to consider the intended use and choose a form or grade that aligns with those requirements. Additionally, individuals or organizations should ensure compliance with regulatory standards and guidelines associated with the use of CDCA in their specific context.

Step 2: Choose a CDCA Source

CDCA is manufactured by pharmaceutical and chemical companies, typically in facilities that adhere to Good Manufacturing Practices (GMP).

Manufacturers of CDCA are often located in regions with a strong pharmaceutical and biotechnology industry. These facilities are equipped with the necessary infrastructure, technology, and expertise to ensure the production of high-quality CDCA that meets regulatory standards.

Some countries that produce CDCA include:


China is a major hub for contract manufacturing organizations that produce active pharmaceutical ingredients (APIs) and other products for the medical industry. While this may offer economic advantages, purchasing pharmaceuticals from China poses inherent risks related to product quality, safety, and regulatory compliance. Concerns about the reliability of quality control standards among different manufacturers have been raised, leading to instances of substandard ingredients, contamination, and inconsistent manufacturing practices. This variability in product quality could endanger the health of consumers, particularly when it involves medications with stringent formulation requirements. 

Additionally, there are concerns about regulatory oversight due to the differences between manufacturers and their adherence to international standards. Mitigating these risks through strong due diligence, supplier vetting, and a commitment to transparent and compliant manufacturing practices is essential when sourcing pharmaceuticals from China.


India is another significant player in the global pharmaceutical industry, with many facilities engaged in API production. While India-sourced pharmaceuticals may have cost benefits, obtaining products may come with risks related to product quality, regulatory compliance, and supply chain integrity. Further, variations in manufacturing standards and regulatory enforcement across different facilities may exist. Instances of non-compliance with GMP, inadequate temperature and quality control requirements, or fraudulent practices have been reported in some cases. These issues raise concerns about the consistency and reliability of pharmaceutical products. 

It is crucial for buyers to carefully assess the reputation and certifications of pharmaceutical manufacturers in India. Further, it is imperative that they are compliant with international regulatory standards, and it is essential to establish clear communication channels to address any quality or safety issues. Thorough due diligence and collaboration with reputable suppliers can help mitigate these risks and ensure the procurement of safe and effective pharmaceuticals from India.


Several countries in the European Union have pharmaceutical manufacturing capabilities, offering numerous benefits to many customers who buy GMP-grade APIs such as  CDCA. 

European suppliers typically adhere to stringent regulatory standards, ensuring the safe production and distribution of high-quality pharmaceutical products. The European Union follows GMP regulations, which set rigorous pharmaceutical manufacturing, testing, and quality control standards, ensuring a high level of assurance regarding product quality and regulatory compliance.

Moreover, European suppliers may offer transparency in their supply chain processes, allowing buyers to trace the origin and manufacturing practices of the pharmaceutical products. This transparency can enhance trust and confidence in the procurement process. Additionally, Europe has a well-established reputation for research and development in the pharmaceutical industry, and suppliers may provide innovative solutions and a diverse range of pharmaceutical products.

When considering CDCA suppliers in Europe, verifying their certifications, compliance with relevant regulations, and reputation within the industry is essential. Engaging with reputable European suppliers can contribute to a reliable and transparent global supply chain, ensuring the procurement of high-quality CDCA for various applications.

Step 3: Ensure Your Source is GMP-Certified

GMP certification is critical when you buy CDCA for several reasons. Firstly, GMP certification ensures that CDCA manufacturing processes adhere to stringent quality procedures. High standards associated with CDCA production include rigorous controls over raw materials, equipment, facilities, and personnel, leading to a consistently high-quality end product. GMP certification is especially vital for substances intended for medical or research purposes, as it guarantees that CDCA meets the necessary purity and safety requirements, reducing the risk of contamination and ensuring its efficacy in various applications.

Secondly, GMP certification establishes a high level of transparency and accountability in the manufacturing process. This assures consumers, research institutions, and pharmaceutical companies that the CDCA supplier is committed to maintaining the highest standards in production. This transparency is essential for regulatory compliance and fosters trust among end-users. GMP-certified CDCA meets quality benchmarks and aligns with ethical and regulatory guidelines, reinforcing its reliability and suitability for use in pharmaceuticals, medical treatments, and research endeavors.

GMP vs. GDP 

GMP (Good Manufacturing Practice) and GDP (Good Distribution Practice) are two critical quality assurance frameworks within the pharmaceutical industry that address specific stages of the product lifecycle. GMP is centered around manufacturing processes, ensuring that pharmaceutical products are consistently produced and controlled to meet quality standards appropriate for their intended use. This involves stringent measures such as proper documentation, validation of processes, adherence to hygiene and cleanliness standards, personnel training, and comprehensive final product testing. GMP focuses on minimizing risks such as contamination, errors, and deviations throughout the manufacturing process, ultimately producing safe, effective, and high-quality pharmaceuticals.

In contrast, GDP is concerned with properly distributing and transporting pharmaceutical products from the manufacturer to the end user. It encompasses the entire supply chain, emphasizing the storage, transportation, and handling of pharmaceuticals to prevent damage, deterioration, or any compromise to their quality and integrity. Key GDP principles involve meticulous documentation of the distribution process, maintaining the integrity of pharmaceutical products during transportation, ensuring proper storage conditions, and implementing quality systems to prevent the entry of faulty medicines into the supply chain. Both GMP and GDP play crucial roles in maintaining the overall quality, safety, and efficacy of pharmaceutical products, addressing different aspects of the complex journey from manufacturing to the hands of the end consumer.

Why Buy GMP-Certified Products?

GMP-certified products are produced and controlled according to standards set by regulatory authorities and relevant industry organizations. 

Quality Assurance

Safety and Efficacy

GMP is a mark of quality. Compliance with GMP standards ensures products are manufactured to high standards, including consistency, equipment, employee training, testing, and facility design. 

GMP-certified products undergo robust quality control and testing procedures to ensure they are consistent, safe, and effective. This is absolutely critical for substances intended for human consumption. 

Regulatory Compliance

Supply Chain Reliability

GMP is recognized worldwide as the leading standard for producing and distributing APIs. Many regulatory authorities, including the European Medicines Agency (EMA), and the US Food and Drug Administration (FDA) require GMP compliance for product approval and marketing.

GMP covers the entire supply chain to make sure your products are top quality from start to finish, including raw material sourcing, storage, and transportation. Choosing GMP-certified APIs ensures supply chain integrity and reduced risk of poor-quality, counterfeit, or contaminated products.

Methylene Blue

About MedicaPharma

MedicaPharma is a trusted and fully licenced API distributor based in Europe that leverages a global network of GMP manufacturers to supply high-quality API’s and pharmaceutical intermediates to healthcare organizations all over the world. 

Different countries and jurisdictions may have varying regulatory requirements, with poor enforcement of relevant rules and regulations. There may be accountability and transparency issues associated with manufacturing and distribution, which increases your risk of receiving non compliant products.

All MedicaPharma APIs are being checked within a closed GDP logistics circuit; in – and outgoing checks secure the quality and supply of the right material.

Trust MedicaPharma For EU-Produced GMP-Grade APIs

MedicaPharma is an EU-based supplier of GMP-certified APIs that serves leading healthcare institutions and research organizations. 


Leverage Our Network of 400+ GMP Manufacturers​

Access High-Quality Chemicals Produced to GMP Standards

Experience Superior  Sales and Support Services

MedicaPharma partners with over 400 leading global producers to supply hospitals, pharmacies, research facilities, and educational institutions.

All our products are produced in regulated, GMP-compliant facilities and shipped with original documentation. No repacking or relabeling. 

MedicaPharma is committed to providing trust, accountability, and transparency. We guarantee our products and support you from start to finish with first-in-class customer service.

Get a Chenodeoxycholic Acid API (CDCA) Quote

Obtaining your desired quotation from MedicaPharma is easy; simply complete the form below to begin processing your quote request.

Please note: MedicaPharma cannot and will not supply customers in the United States due to commercial restrictions.

"*" indicates required fields

Please mention desired volume, project background and specific requirements.

Step 4: MedicaPharma Your Qualified Supplier

Finding a reliable supplier when you buy GMP-grade APIs like  CDCA is crucial, especially when it’s intended for medical, research, or industrial purposes. 

MedicaPharma is your GMP API grade CDCA partner:

Regulatory Compliance

MedicaPharma complies with relevant regulatory standards and guidelines. Depending on your location and the intended use, CDCA may be subject to specific regulations. 

Supplier Reputation

Research the reputation of MedicaPharma in the global pharmaceutical market. Look for reviews, testimonials, or references. We have a track record of many cases studies, please feel free to contact us to give examples. 

As a EU based company, we provide reliable and high-quality products.

Quality Assurance

Inquire about the MedicaPharma’s quality control and assurance processes. We are happy to provide information on the testing methods used to ensure the purity and quality of the CDCA products.

Shipping and Logistics

MedicaPharma is shipping worldwide; please discuss our shipping capabilities and logistics when you buy CDCA. Reliable shipping methods and proper packaging are crucial to ensure the safe and timely delivery of your order. We have years of experience in this field.

Certifications and Relevant Documentation

MedicaPharma holds relevant documentation related to product quality, including a Certificate of Analysis (COA), GMP certificate, Material Safety Data Sheet, and accelerated stability data. We are a worldwide Niche API Specialist and supply to all GMP regulations.

Customization and Formulations

If you have specific formulation requirements, please inquire with us to customize CDCA formulations to meet your needs. Customization is essential, especially if you require a particular grade or formulation for your application.

Supply Chain Reliability

Discuss with us the  pharmaceutical supply chain capabilities before you buy CDCA. We have a stable supply chain in place to ensure consistent product availability. Inquire about our production capacity and backup plans in case of unforeseen disruptions.

Communication and Support

Evaluate MedicaPharma’s communication channels and customer support. A responsive supplier that communicates effectively is more likely to promptly address any concerns or queries. We are EU based, reliable and our goal is to always answer enquiries within 24-hours. We believe in building a long-term cooperation.

Cost Considerations

While cost is a factor, it should not be the sole determining reason when buying CDCA. Balance cost considerations with MedicaPharma’s reputation, quality assurance, and other factors to ensure overall value.

Contract and Terms

Review our terms of the contract carefully. Ensure it includes details about product specifications, pricing, delivery timelines, and other relevant terms.

CDCA Buying Guide FAQ

The medical industry uses CDCA (Chenodeoxycholic Acid) for various applications in medicine and research. These include medications to treat conditions like gallstones and liver disorders, and for biotechnological research for diabetes treatment.

CDCA can come in different forms, including pharmaceutical grade for medical applications, research grade for laboratory studies, and various formulations such as capsules, tablets, microencapsulated forms, and combination formulations.

CDCA is manufactured by pharmaceutical and chemical companies, often in regions with strong pharmaceutical and biotechnology industries. Common manufacturing locations include China, India, and Europe.

Sourcing pharmaceuticals from China may pose risks related to product quality, safety, and regulatory compliance. Variability in manufacturing practices and concerns about quality control standards require thorough due diligence when selecting suppliers in China.

Sourcing pharmaceuticals from India comes with potential risks related to product quality, regulatory compliance, and supply chain integrity. Variations in manufacturing standards and non-compliance may exist, emphasizing the need to assess suppliers in India carefully.

Buying CDCA from Europe offers potential benefits due to adherence to stringent regulatory standards, transparency in supply chain processes, and a well-established reputation for research and development in the pharmaceutical industry.

Choose a CDCA supplier that complies with regulations, has a strong reputation, and adheres to quality assurance processes and certifications. Other factors to consider include customization options, supply chain reliability, costs, and shipping policies.

EU-based supplier MedicaPharma provides high-quality APIs and pharmaceutical intermediates to leading sales, research, and education institutions. Click here to request a quote.

Recommended articles