About Europharma

EUROPHARMA ALLIANCE IS A LEADING EUROPEAN CONTRACT MANUFACTURING ORGANISATION OFFERING VARIOUS PRIVATE LABEL FORMATS INCLUDING CAPSULES, BOTTLES, SACHETS, BLISTERS AND MORE. OUR MODERN MANUFACTURING FACILITY IS LOCATED IN RZEPLIN, POLAND.

OUR ACTIVITIES, APART FROM CONTRACT MANUFACTURING INCLUDE

 

Order processing
Quality Assuranace
B2B Sales & Promotion
Regulatory Affairs
Account Management
Logistics & Distribution

 

tagi

 

Services

powdersPowders & Semi-Powders

Mixing and packing into stick sachets. The process is handled in a dust free environment using vacuum conveyors on each stage. There are weighing modules and metal detectors installed at critical points of the process. Raw materials are also sieved before mixing. Mixing efficiency is validated. Ready sachets are checked regularly for their tightness using a water vacuum tank. Our annual capacity is up to 80 million sticks.

blisteringBlistering and cartoning line

We processes tablets, hardgels, softgels and chewable products. We have installed camera system to automatically reject faulty blisters. Our machines can be easily adapted to new formats, making it simple for us to offer our customers packing measurements tailored to their individual needs. The new tooling is provided free of charge. Our annual capacity is up to 60 million blisters

 

jarJar and Bottle Filling

Our packaging lines are suitable for filling jars and bottles made of plastic, glass or aluminum with capsules and tablets. Additional line facilitates fill of liquids and semi-liquids into bottles with volumes ranging from 20 – 1000 ml. Both lines are complemented with labelling and capping machines. Annual capacity is estimated at 45 million plastic jars and 2.5 million bottles (as per 300ml).

 

hard gelatinHard Gelatin Capsules

We offer automatic fill of hardgels with powders and pellets. Available sizes are 1, 0, 00, 000. We work on shells made of gelatin as well as of plant origin. Line capacity is 225 million capsules annually.

 

tabletsTablets

Starting from 2018 we offer full scope of tableting services including wet granulation in fluid bed dryer and tablet water based coating. Our team is made of technologists with long experience in formulation of dry dosage forms. The hi-tec tableting line is brand new and has been partially financed with EU grants. Estimated capacity is approx. 75 million tablets annually.

Products

bg products

Access to information is a key driver for innovative solutions. Using more than 10 years experience in private label business as well as permanent presence on leading Shows and Exhibitions we bring value to locally oriented companies which can turn our innovation into their own market competitiveness.

Our line of products reflects the latest market trends and takes into consideration ever changing regulatory conditions. Our concepts revolve around two main ideas:

1. to significantly improve existing , well established products giving our clients required competitive edge.

2. to offer completely new products, which answer current market needs and fit into existing or future regulatory framework.

Our current product catalogue is available here.

Quality

ico qualityQUALITY CERTIFICATION
isoMEDICAL DEVICES and FSMP
ico qualityREGULATORY COMPLIANCE

Europharma Alliance is a holder of FSSC 22000 certificate issued by TÜV Rheinland Cert GmbH,
a leading provider of technical services worldwide. The FSSC 22000 Food Safety System Certification provides a framework for effectively managing organization’s food safety responsibilities. FSSC 22000 is based on existing ISO Standards and demonstrates that company has a robust Food Safety Management System in place that meets the requirements of customers and consumers.

Europharma Alliance has implemented an ISO 13485 system for Medical Devices which is integrated with FSSC 22000 and serves as an extension to the latter.

This enables the company to offer product development and contract manufacturing of both food supplements and medical devices.

Europharma Alliance provides under Technical Agreements all necessary measures to bring the products of our clients to the compliance with current EU food safety regulations. This includes product risk assessment, control of environment impurities, stability testing. All the stages of production, warehousing as well as transportation are monitored for temperature and humidity. Batch records and retention samples are stored in controlled conditions. All routine checks are performed in our in-house laboratory, more complex tests are made in independent GLP laboratories.

EU Funds