PDG Consulting: Solutions for the pharmaceutical industry

Nations around the world have enacted laws to improve patient safety and prevent counterfeit drugs from entering the supply chain. Many of these regions have their own unique requirements, which add several layers of complexity for pharmaceutical manufacturers, distributors, and retailers.

We believe that our expertise in these markets will allow us to advise you on the most suitable solution for your business, meeting the requirements of each market. As regulations change, manufacturers must stay up to date to ensure that their products meet the highest standards of safety and traceability. 

Whether in Europe, where the Falsified Medicines Directive (FMD) requires a serialization system, or in the United States, with guidelines imposed by the FDA, each region presents unique challenges.

Our pharmaceutical regulatory compliance experts are equipped with the tools and knowledge to help companies navigate this complex regulatory landscape. 

By offering consultancy services on a global scale, we help our clients to optimise their supply chain, reducing the risk of counterfeit products and improving the traceability of their medicines. In addition, we ensure that their processes are transparent, efficient and comply with all local and international regulations.