Cooperation
Contract services
Serialization
LABOR is prepared to implement the provisions of Directive 2011/62 / EU of the European Parliament and of the Council of 8 June 2011 on the Community code relating to medicinal products for human use – in terms of preventing the introduction of falsified medicinal products into the legal distribution chain as well as Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83 / EC of the European Parliament and of the Council by laying down detailed rules concerning safety features placed on the packaging of medicinal products for human use.
We place serialization security on packages of medicinal products: 2D code, package integrity element and a serial number registered in the database of the KOWAL Foundation, which is the system operator in Poland.
We offer the possibility of using our services in the field of placing security features on the packaging of medicinal products for human use.
Manufacture of non-sterile forms of medicinal products
- round, oval, convex tablets, with or without a break
- lozenges
Manufacture of dietary supplements:
- round, oval, convex tablets, with or without a break
- lozenges
Labeling and packaging
- medicinal products
- dietary supplements
- food products
- cosmetics
More services:
Packing in Alu / PVC blisters and PP, HDPE containers
Mixing, granulating, briquetting and tabletting
Development of compositions and recipes for medicinal products, dietary supplements and cosmetics
Tableting and confectioning of household chemicals
Development of registration documentation and a system for ensuring GMP and HACCP requirements
Comprehensive chemical analysis of materials and products (including HPLC, UV-Vis, release testing apparatus)
Comprehensive microbiological analysis of the purity of materials and products
Comprehensive microbiological analysis of air and surface cleanliness
Development of quality specifications, analytical methods and their validation
Synthesis of active pharmaceutical ingredients (API) in the GMP standard
Are you looking for a manufacturer?
We provide services in the development and production of pharmaceutical and chemical products. The scope of work depends on your decision.
Visit us
49 Długosza str.
51-162 Wrocław, Poland
Reporting of Adverse Drug Reaction for the patient
Reporting side effects for the heathcare professional
Call us
+ 48 71 325 30 85/86