Who We Are?
We are a Polish and independent family-owned company, which dates back to 2000. Our office is located in the historical district of Wilanów, Warsaw. The enterprise was initially run as a sole proprietorship, and on the 20th anniversary of its establishment, it was transformed into a limited liability capital company, still fully owned and managed by the founding family.
What we do?
Our focus is centered on selected industries and products. This strategic focus allows us to generate added value for manufacturers cooperating with us and guarantee the highest level of service to our customers. We specialize in the import and distribution of active pharmaceutical ingredients (APIs) and other key raw materials & ingredients for the pharmaceutical industry as well as specialized components for the food industry, with special properties or performing specialized functions. Some of our products are also used in the cosmetics and veterinary industries.
PHARMACEUTICAL QUALITY
PHARMACEUTICAL QUALITY
Our procedures, processes and standards are formalized within our pharmaceutical quality management system. We are certified by the Polish Chief Pharmaceutical Inspectorate in terms of Good Distribution Practice and are subject to regular audits. We are authorized to import and distribute APIs used in the production of medicinal products in the European Union. Moreover, regardless of the final application of distributed substances – whether it is the pharmaceutical, food (including dietary supplements), cosmetic or veterinary sectors – we operate on the basis of standard operating procedures and a quality management system supervised by pharmaceutical authorities and based on the assumptions of the PN-EN ISO 9001:2015 standard.
QUALIFIED SUPPLIERS
QUALIFIED SUPPLIERS
In accordance with our quality management system, manufacturers of APIs and subcontractors of key processes and services (including storage and transport) are subject to formal qualification, an audit scheme and periodic assessment. The processes of supplier qualification and supplier supervision ensure that subcontractors are able to provide services of the required quality and that API manufacturers are able to manufacture and deliver a pharmaceutical substance in accordance with the requirements of the Polish/EU pharmaceutical law and the individual requirements of the final recipient, and that their quality assurance system guarantees full control and repeatability of quality parameters.
RARE & SPECIALISED SUBSTANCES
RARE & SPECIALISED SUBSTANCES
Our offer includes a wide range of unique substances. We are licensed to import and distribute products of animal origin and animal by-products of category 3 intended for use, among others, in in the manufacturing process of medicinal products, medical devices (including active implantable devices and devices used for in vitro diagnostics), cosmetic and veterinary products. We have experience in trading products with ADR status, flammable and requiring controlled temperature and humidity conditions (e.g. active substances for vaccines).
FLEXIBILITY AND AGILITY
FLEXIBILITY AND AGILITY
Our organization easily adapts to all changes in the environment. We act quickly and without unnecessary bureaucracy. Most deliveries are made directly from the manufacturer to the individual order of the final recipient. Reducing the number of stages in transport and storage places allows us to minimize the quality risk. In addition to the substances in our permanent offer, we also provide dedicated search services for rare substances or substances with specific quality requirements. We are able to analyze the market in a short time and identify potential producers for any raw material.
How do we operate?
On individual product markets, we work closely with selected and previously qualified manufacturers from third countries and from the European Union. This cooperation is usually based on the principle of exclusive representation and long-term partnership, in order to provide our clients with products and after-sales services of the highest quality. We create a friendly environment for the two-way flow of information between producers and end users. We have access to full registration documentation of the offered products, which in the case of APIs includes, among others: ASMF/CEP, GMP, Written Confirmation (if applicable) and all additional manufacturer’s statements.
Our comprehensive services for pharmaceutical industry include:
Search for new sources of API supplies
Search for alternative sources of API supplies
Adjustment of API specification to the predefined requirements of specific projects
Full project documentation support
Organization of GMP audits at API manufacturers
Supply chain monitoring and supervision
