One of the challenges of the pharmaceutical industry worldwide is to reduce the falsified medicines and guarantee the patient’s security. The UE has created a regulation, which will be effective in 2016, with the aim of stopping the introduction of unidentified products into the supply chain. The establishment of this regulation will have a big impact on the coding and identifying process of the pharma products. That means that 80% of the coding solutions currently used will become obsolete when the regulation is effective.
Much more than a software
SERIAL FARMA is a global solution to adapt the company to the FMD regulation and it is made up of following stages:
• Consultancy and advising to choose the systems and equipments.
• System controlling and management through the SERIAL FARMA software: marking systems, 2D codes reading systems and printing quality control and OCR/OCV Vision systems to validate the “humanly readable” alphanumerical codes.
• Data base management according to the FMD regulation.
The SERIAL FARMA Software provides a solution that combines the high technology marking laser systems with advanced IT systems by means of a complete solution at all levels: management, production and serialization coding.