On Monday, Recipharm announced it had shipped several batches of drugs to Saudi Arabia, explaining the products were labelled in accordance with serialization rules introduced in November in the latest version of the Saudi Drug Code.
In order to comply with the new rules – which came into effect last month – Recipharm had to install technology at its manufacturing site in Lisbon, Portugal.
Marchesini and SEA Vision provided the hardware and software according to Staffan Widengren, director corporate projects at Recipharm, who told us the investment fitted with the firm’s wider €40m serialization capacity effort.
“This project at our site in Lisbon is part of Recipharm's global serialisation program and it requires steering from central stakeholders as well as support from vendors of equipment, hardware and software.”
Widengren added that: “From the local site it is important to engage all functions that are involved in the process of packaging including serialisation, release and distribution of batches independent of markets.”
Like other serialization requirements elsewhere, the Saudi rules are designed to prevent counterfeit products entering the supply chain.
Drug companies are required to replace linear barcodes with GS1 DataMatrix barcodes, which include a unique product identifier, batch number, expiry date and serial number.
Clinical manufacturing expansion
In other news, Recipharm opened a manufacturing suite for clinical trial materials at its facility in Research Triangle Park, North Carolina, US.
The facility, which cost $750,000, is designed to supply non-sterile dosage forms, semi-solid topical drugs and products in metered dose inhalers for customers running Phase II trials.