Safely moving drug products requires new ways of thinking and working — with technology.

Regulations are nothing new to the pharmaceutical industry. They’ve been around since the early 20th century and have continued to evolve ever since, with regulators such as the U.S.  Food and Drug Administration (FDA) and the European Medicines Agency (EMA) in the EU ensuring the safety, efficacy and quality of pharmaceutical products.  

But the regulatory landscape constantly changes, including increased scrutiny around environmental conditions in the storage and transportation of pharmaceuticals and biologics. It’s imperative to have proven systems and processes in place in order to comply with all requirements.   

As a result, Good Manufacturing Practices (GMP) have become a prerequisite for conducting business as the pharma industry works to ensure regulations are implemented and processes are validated. Keeping up to speed with the ever-changing global regulatory environment is enough to make anyone’s head spin — yet it’s non-negotiable when it comes to ensuring ongoing compliance. Read more >