26. May 2023

Trade fair PLMA 2023 in Amsterdam

From May 22nd to 24th we were active as an exhibitor at the PLMA trade fair in Amsterdam. At this world's largest private label event, we met customers, business partners and interested parties at our colourful and inviting booth under the motto "Inspirations & Solutions". With various collections of fragrances, essential oils and flavours, we were able to convince our numerous guests with competence and creativity. A great time for valuable conversations and highly informative exchange in an inspiring environment! Many thanks to all who visited us.
06. March 2023

Support for “Help Mada”

Since the beginning of this year FREY&LAU supports with great pleasure the non-profit association "Help Mada e.V.". In this way, we would like to make a contribution to sustainably improving the quality of life of the people of Madagascar. About 80% of the population there live below the poverty line. What is particularly lacking is adequate medical care and educational opportunities. "Help Mada e.V." collects donations to build and expand schools and health stations. In addition, vanilla farmers are to be provided with an additional source of income through vegetable cultivation. FREY&LAU has been sourcing vanilla pods from Madagascar for decades, which we process at our site.


13. January 2023

Good news

19. December 2022


01. September 2022

Summer Festival 2022

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Fi Europe

28. - 30.11.2023 / Paris

Gulfood Manufacturing

07.-09.11.2023 / Dubai


31.10.-02.11.2022 / Dubai
Hall Sheikh Saeed 2, booth A35


25. - 27.10.2023 / Berlin


24.10.- 26.10.2023 / Barcelona

CarwashPro 2023

21.- 22.09.2023 / Amsterdam

PLMA 2023

23.- 24.05.2023 / Amsterdam

Pharma / GMP

As a leading manufacturer of essential oils that are suitable as active pharmaceutical ingredients (API), we ensure compliance with the highest standards when it concerns consumer protection and product safety for use in pharmaceuticals. We are producing for our customers within the scope of our European GMP certificate under GMP II active ingredients and are offering under our EGST-Line Eucalyptus oil GMP, Turpentine oil GMP, Peppermint oil GMP as well as several others. Because of our manufacturing license according to § 13 AMG we are able to produce high-quality pharmaceutical intermediate products under GMP I. For the approval process, product registration and to facilitate a fast market launch of our customers’ products, we offer complete ASMF solutions and documentation packages, as well as stability tests according to ICH Guidelines.




The following product list will provide you with an overview of the essential oils that are suitable for use in pharmaceuticals.


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GMP Manufacturing of Active Ingredients

Drug safety at the highest level: Active pharmaceutical ingredients (API) used in the production of pharmaceuticals must be manufactured in compliance with the Good Manufacturing Practice (GMP) principles. FREY&LAU fulfills all applicable requirements with a corresponding quality assurance system and is accordingly GMP-certified by the responsible authority. We are in possession of the manufacturing authorization for pharmaceuticals registered under the Eudralex Database, pursuant to § 13 AMG, which includes the authorization for further treatment of pharmaceutical intermediate products. Our GMP certificate enables us for essential oils and their constituents, to distil them, and to implement any additionally required steps necessary for the production and sale of essential oils as active pharmaceutical ingredients (API). Our product range currently encompasses 15 essential oils in API Quality.


The simple route to register pharmaceutical products: We want to effectively and efficiently support our partners through the drug approval process. To this end, we offer comprehensive packages of qualified documents for seamless and transparent documentation. For the approval of essential oils as active ingredient components in pharmaceuticals, we create corresponding dossiers in our approval department for all active ingredient products in accordance with the European Drug Master File Procedure (ASMF). This allows us to meet the continuously growing challenges of European legislation. Moreover, we advise our customers extensively in direct contact with the responsible approval authorities, thus supporting numerous approval proceedings every year, all across Europe.