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Prescription and OTC Drugs
We Help Prevent Problems, Deliver Speedy Solutions
Many large corporations produce OTC and prescription drug products. However smaller businesses actually constitute a large majority of the FDA-regulated industry. Our firm works with small and medium-sized clients to assure that the impacts of all regulatory requirements are understood and that adverse impacts are lessened whenever possible, before regulations are issued.
Our Food and Drug lawyers counsel clients on the following:
- New Prescription Drug Approvals;
- Establishment Inspections;
- Laboratory Validation;
- Sterility;
- Import and Export of Drugs;
- Promotion and advertising;
- Over-the-Counter Drug Information;
- Drug Safety & Side Effects;
- Drug Preparedness and Bioterrorism Response;
- Clinical Trials;
- IRBs;
- Warning Letters; and
- Registration and Listing - Domestic and Foreign.
Helpful Links
Guidance for Drug ApplicationsHow Drugs are Developed and Approved
Small Business Assistance
Import/Export of Drugs
Drug Manufacturing
Drug Registration
Post-Market Requirements Contact Us for an initial consultation