Chr. Olesen Group

About

The Chr. Olesen Pharma division distributes human and veterinary APIs to the global pharmaceutical industry. We source our APIs from qualified manufacturers worldwide, as well as from our own factory, Chr. Olesen Synthesis A/S, in Denmark. Our comprehensive range of services encompasses every aspect of active pharmaceutical ingredients, including import, warehousing, sales and distribution, marketing, product and business development, and quality management. With decades of experience in this field, we are able to meet our customer’s needs for the production of their pharmaceutical finished formulations.


 

What do we do now?

Today, Chr. Olesen’s Pharma division is divided into two business areas: APIs and Intermediates. We have offices in Denmark, Belgium, Brazil, Germany, and the USA and primarily distribute our...

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Address: Jægersborg Allé 164, 2820, Gentofte
Denmark
Denmark Local time:

Trusted for 140 years

Global distribution business with API manufacturing facilities

European company with presence in 3 continents

Our services:

APIs
Intermediates
Controlled substances
Vitamine

Response time:

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Employees:
150
Established in:
1885
Number of products Number of products:
89

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Chr. Olesen Group is a supplier from Denmark. They offer 89 products (APIs, Excipients or Intermediates). Contact Chr. Olesen Group for free and get a competitive price offer.

Find a price of Acetylsalicylic acid bulk with GMP, CEP offered by Chr. Olesen Group.
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Find a price of Methylcobalamin bulk with GMP, USDMF offered by Chr. Olesen Group.
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Find a price of Sulfadiazine Sodium bulk with GMP, CEP offered by Chr. Olesen Group.
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Find a price of Trimethoprim bulk with GMP, CEP offered by Chr. Olesen Group.

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Are you looking for pharmaceutical ingredients for the production of medicines? Contact the supplier of your choice by using the send inquiry button and find out how much it cost. The supplier will contact you with their price and conditions. Chr. Olesen Group replies quickly.

You can send an inquiry for these products. Some suppliers have set a minimum order quantity (moq). Provide enough information regarding your enquiry. Let Chr. Olesen Group know whether you are looking for Ph.Eur (EP), USP, BP, JP grade. Also, let the manufacturer or trader know if you are looking for hydrochloride (HCl), base or other product specifications. Is it for own production, resale or research purposes? Contact Chr. Olesen Group, get a price, download certificates and buy the product.

Chr. Olesen Group


About

The Chr. Olesen Pharma division distributes human and veterinary APIs to the global pharmaceutical industry. We source our APIs from qualified manufacturers worldwide, as well as from our own factory, Chr. Olesen Synthesis A/S, in Denmark. Our comprehensive range of services encompasses every aspect of active pharmaceutical ingredients, including import, warehousing, sales and distribution, marketing, product and business development, and quality management. With decades of experience in this field, we are able to meet our customer’s needs for the production of their pharmaceutical finished formulations.


 

What do we do now?

Today, Chr. Olesen’s Pharma division is divided into two business areas: APIs and Intermediates. We have offices in Denmark, Belgium, Brazil, Germany, and the USA and primarily distribute our products to Europe, Africa, Latin America, and the USA. The pharmaceutical business is currently led by Managing Partner Tobias Facklam.

 

 

How did it start?

As a distributor of feed and food ingredients, it was a natural progression for Chr. Olesen to expand into distributing ingredients for the veterinary pharmaceutical industry. The journey of distributing pharmaceutical ingredients started in 2006. Since then, we have further gone into the human API market and later into exclusive intermediates for pharmaceutical applications.

 

 


 

Quality Management System

We have a well-implemented quality management system (QMS) that follows current international rules, specifically the EU-GDP (Good Distribution Practice) and EU-GMP (Good Manufacturing Practice) guidelines. The QMS ensures complete and compliant documentation for the APIs, in accordance with regulatory requirements such as those of EMEA, EDQM, FDA, and other local authorities.