Imagine the value of continuous access to the specialty pharmaceutical consulting services and resources necessary to complete tasks that are out of the ordinary, unexpected, or for which you just don’t have time. Most of our clients do not have the resources to execute each facet of every project they take on, or might otherwise face.
Unexpected events such as product licensing opportunities or newly proposed FDA regulations may demand immediate attention and expertise. Service to our clients in situations just like these has taught us that successful companies are always positioned to address such challenges. PDG provides a wide variety of drug consulting competencies and capacity through our specialty services that will help you to do so with immediacy and quality. In addition to those drug consulting services listed below, PDG will help you conduct safety assessments, issue Dear Healthcare Professional Letters, review new promotional labeling, place studies, design or edit study protocols, address IRB and data or safety monitoring concerns.
PDG offers a wide range of drug consulting specialty services as your long-term regulatory partner throughout the lifespans of your products. Given our versatility, it should come as no surprise PDG has completed a large number of diverse projects for our clients. We provide a multitude of additional consulting services, the most popular are reflected in the list that follows. If there is a service you need (but do not see) relating to a drug product, contact us so we may discuss it.