structured on solid scientific and modern concepts, along with successful marketing management.

We have a wide range of high quality products that are manufactured in all over the world and exported to the Middle East. Our expertise expands to a wide variety of categories including, but not limited to; Food supplements and natural pharmaceuticals, Herbal Raw Materials, APIs, Veterinary materials, excipients & Vitamins with GMP certified manufacturers. We are confident that through our professional team of pharmacists, doctors, marketing experts and through the location of our branches, D-NEW PHARM will successfully continue to grow and expand internationally.

As part of its business strategy,

D-NEW PHARM has a fully dedicated Export & Import Department that is committed to this important task, its main goal is to provide strategic oversight to its business partners located in over 28 countries in the Middle East, Africa, Asia and Eastern Europe.

In the pharmaceutical industry,

Quality Management is usually defined as the aspect of management function that determines and implements the (quality policy) i.e. the overall intention and direction of an organization regarding quality, as formally expressed and authorized by Top Management.

Although we support our customers with APIs

and INACTIVE EXCIPIENTS ingredients, but we decided to support the D-NEW PHARM clients from the very beginning, by offering the required brand for them to proceed with their stability tests and bio-equivalence studies. D-NEW PHARM technical teams are experts in sourcing and supplying pharmaceutical brands and biologicals. D-NEW PHARM supports and supplies the customers with pharmaceutical brands from different regions and reference countries all over the world (North America, Europe & Australia). Our Account managers and sales representatives are willing to provide the required services with the best price and quality and that’s the corner stone of D-NEW PHARM success. With the loyalty of an ever-increasing customer base, our company will remain in priority.

A drug reference standard is a standardized

substance which is used as a measurement base for similar substances. Where the exact active substances of a new drug are not known, a reference standard provides a calibrated level of biological effects against which new preparations of the drug can be compared. We are a leading global distributor of reference materials and proficiency testing schemes. We supply reference standards from BP, USP, LGC and other manufacturers. These high quality products and services are essential for accurate analytical measurement and quality control, ensuring sound decisions is made based on reliable data.