Regulations like the EU’s Falsified Medicines Directive and the DSCSA provisions of the US FDA’s DQSA have become a major hurdle for the global pharmaceutical industry- compliance has become complex in the extreme and efforts at achieving global standardization have not had the impact that is needed to ensure that compliance is made quickly, efficiently and in a cost effective manner. The ongoing and rapid changes that are constantly taking place with research and development turning out new products on an ongoing basis globally, combined with nationally based protectionist legislation helps to ensure that the burden of tracking and accurately labeling a product so that it can get into new markets lies entirely on the shoulders of the company making the goods.

Data management is essential to survive in this kind of complex and ever evolving environment. Properly done, it will help ensure that materials are accurately inventoried, efficiently transported and delivered on time. Good data management will also help to identity bottle necks and costly inefficiencies that can then be death with,

Efficient and accurate labeling processes are critical to e-pedigree program deployment and serialization.  Having a secure, scalable and easy to use labeling system that allows you to easily track and trace is while keeping up with the constantly changing regulatory environment is the competitive edge that any pharmaceutical company needs to survive and thrive.