Traceability of Biologics in The Netherlands: An Analysis of Information-Recording Systems in Clinical Practice and Spontaneous ADR Reports

Effect of barcode technology with electronic medication administration record on medication accuracy rates

(2014) H. H. Seibert et al.   AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY

Recombinant factor VIII products and inhibitor development in previously untreated boys with severe hemophilia A

(2014) T. Calvez et al.   BLOOD

Safety Profile of Biological Medicines as Compared with Non-Biologicals: An Analysis of the Italian Spontaneous Reporting System Database

(2014) Paola M. Cutroneo et al.   DRUG SAFETY

Traceability of biologicals: present challenges in pharmacovigilance

(2014) Niels S Vermeer et al.   Expert Opinion On Drug Safety

Traceability of Biopharmaceuticals in Spontaneous Reporting Systems: A Cross-Sectional Study in the FDA Adverse Event Reporting System (FAERS) and EudraVigilance Databases

(2013) Niels S. Vermeer et al.   DRUG SAFETY

EU’s New Pharmacovigilance Legislation: Considerations for Biosimilars

(2013) Begoña Calvo et al.   DRUG SAFETY

Evaluating the Completeness and Accuracy of MedWatch Data

(2012) Kenneth A. Getz et al.   AMERICAN JOURNAL OF THERAPEUTICS

Acceptable changes in quality attributes of glycosylated biopharmaceuticals

(2011) Martin Schiestl et al.   NATURE BIOTECHNOLOGY

Effect of Bar-Code Technology on the Safety of Medication Administration

(2010) Eric G. Poon et al.   NEW ENGLAND JOURNAL OF MEDICINE