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Quality


R& D - Product development
Because trends are always changing in our market, DuSart Pharma has perfected the ability to respond to the latest developments. We possess the know-how and expertise to translate ideas into concrete products that stand out in the market place. All formulas for new products are based on scientific research and literature, and focus on ‘Unique Selling Points’ (USP).

Our philosophy is to develop successful products in close collaboration with our customers. We are experts in “translating” existing products to meet EU guidelines or can help customers to develop new products for a specific market/customer/target group. As brand owner, we take part in the product development process, which helps us to offer maximum help and assistance to our customers. DuSart Pharma continuously keeps abreast of the very latest developments in terms of laws and regulations. This know-how allows us to develop products that comply with the strict requirements established by the government in the Commodities Act. Our “Research & Development” team consists of experienced specialists and is supervised by a qualified pharmacist.


Laboratory


DuSart Pharma possesses an up-to-date in-house laboratory which, thanks to a wide range of technology, can guarantee that forgeries of raw materials are detected and that only raw materials with the correct identity are used. Further, in-process checks are also carried out at the laboratory. A professional team of Quality Controle employees helps to safeguard the quality of the product.


Quality Assurance


DuSart Pharma has an extensive Quality Assurance System. The “Dry dosage forms” (tablets, capsules and powders) department at DuSart Pharma is subject to the GMP norms for food supplements, in accordance with the Quality Guide issued by the EHPM*. By complying with these strict norms, DuSart Pharma also meets requirements established under the HACCP. The “Liquid dosage forms" department is also responsible for producing homeopathic medicines. The department is thus subject to the strictest norms. DuSart Pharma possesses the required GMP permit: “ GMP-Certificate Nr: NL/H 09/0051” issued by the Health Care Inspectorate. The products that are exported to the United States of America have been approved by the FDA.

*EHPM stands for: European Federation of Associations of Health Product Manufactures website: www.ehpm.org


DuSart Pharma b.v.
for all your private labels
;

- Homeopathy
- Herbal Tinctures
- Liquid formulations
- Tablets
- Capsules
- Ointments
- Filling
- Full service concept
- Product development
- Marketing & Communication
- Nutraceuticals
- Contract blistering


Questions?
Call us for more information



Private label - Homeopathy - Herbal tinctures - Liquid formulations - Tablets - Capsules

- Ointments - Filling - Full service concept - Product development -

Marketing & Communication
- Nutraceuticals - Contract blistering
DuSart Pharma b.v. - Nijverheidstraat 15 - 2222 AV Katwijk ZH - P.O.Box 3219 - 2220 CE Katwijk ZH - The Netherlands
T (+31) 71 402 86 64 - F (+31) 71 402 84 24 - E-mail: info@dspharma.nl www.dusartpharma.com
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