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 must complete.
Unexpected events such as product licensing opportunities or newly implemented 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. Biotech Research Group is one of a few pharmaceutical consulting firms that provides a wide variety of drug consulting competencies through our specialty services that will help address any regulatory needs with immediacy and quality. In addition to the drug consulting services listed below, Biotech Research Group 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.
Given our versatility, it should come as no surprise Biotech Research Group has completed a large number of diverse projects for our clients. We provide additional consulting services, and the most popular are reflected in the list that follows. If there is a service you need (but do not see) relating to drug product or medical devices, contact us so we may discuss it.
- Literature Searches
- Pharmacokinetic Consulting
- Scientific, Medical and Technical Writing
- Legal Services
- Toxicology Consulting
- Clinical Trials
- FDA Fast Track Program
- OTC Drugs
- Dietary Supplements
- Citizen Petitions
- USAN Chemical/Drug & Biologic Brand Naming
Of the pharmaceutical consulting companies, only Biotech Research Group offer a responsive, wide range of drug consulting specialty services and will be your long-term regulatory partner for the lifespans of your products.