Strong regulatory strategies are pivotal in getting products to market. While many countries’ drug regulations are similar, there are still significant differences. These similarities and differences are the basis of a global regulatory strategy that encompasses the needs of all regions. Serving you where you need to be, our Regulatory Affairs teams are located throughout North America, Latin America, Asia Pacific and Europe.
As global regulatory requirements continue to evolve, Covance’s expertise helps you increase your chance of regulatory approval. With over 150 regulatory affairs professionals in more than 14 countries around the world, we help you navigate regulatory requirements throughout your product’s development lifecycle.