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Ace Biopharm inquiries: raw material quotations, contract manufacturing (CDMO) and careers
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Thank you for your interest
in Ace Biopharm.
We welcome your queries and feedback.
Frequently Asked Questions
What kinds of ingredients do you supply?
We supply active pharmaceutical ingredients (APIs), excipients, food ingredients, cosmetic ingredients, and wholesale ingredients. A total of 239 products are currently listed on our website: 79 KDMF APIs, 15 excipients, 86 food ingredients, 59 cosmetic ingredients. For APIs, we have registered DMFs for a cumulative total of 248 products (as of August 2026). Each product has its own page, where you can check the ingredient name, CAS No., KDMF registration number, manufacturer, and specifications.
Can I search for ingredients by name or CAS number?
Yes. Simply enter the ingredient name (in English or Korean) or its CAS number into the search bar on our Products page. You can narrow results using filters such as product category, specification standard (EP, USP, KP, NF, JP, BP, or In-House), and manufacturer. You can also bookmark or share specific search result URLs directly with colleagues.
How can I check whether an ingredient is KDMF-registered?
Filter your search by selecting "KDMF Registered Only" in the product catalog. The dedicated product detail page displays the official registration number. If no registration number is shown, the item is not currently registered under KDMF.
How do I request a quotation or a sample?
On the Contact page, select the "Raw Material Quotation" inquiry type and enter the products you are interested in (ingredient name or CAS No.) along with the quantity required. Our team will review your request and reply. You can select any combination of quote, sample, and technical documents. If you add several products from the product list and request them together, the product field is filled in automatically.
Do you also offer contract manufacturing (CDMO) services?
Yes. Through our strategic partnership with Porton—a global CDMO—we utilize cGMP-compliant manufacturing infrastructure certified by the US FDA, EMA, and PMDA. We deliver end-to-end services from API sourcing and process development to chemical synthesis and finished dosage form (FDF) manufacturing. Our capabilities span early preclinical stages through commercial production, and we gladly execute Non-Disclosure Agreements (NDA) upon request.
Do you manufacture any ingredients in-house?
Yes. At our Pyeongtaek plant, we manufacture bio-based ingredients such as vitamin K2, probiotics, and amino acids in-house through fermentation and purification processes. The plant began operating in November 2021, holds FSSC 22000/ISO 22000 and Kosher/Halal certifications, and comprises a production facility of approximately 1,650 m² on a site of approximately 8,260 m². Technologies developed for commercialization at our Daejeon Bio R&D Center (established in 2019) are carried through to production at this plant.
How do you manage quality and storage?
At our Hwaseong logistics center, ingredients are stored and shipped in accordance with KGIP and KGSP standards. In 2018, our in-house testing laboratory received KGIP certification from the Seoul Regional Office of Food and Drug Safety, and we hold 12 certifications in total, including Kosher and Halal. Certification details and DMF registration status are available on the Quality Control page.