What is general pharmaceutical?
In the United States, the Food and Drug Administration (FDA) is responsible for creating guidelines for the approval and use of drugs. The FDA requires that all approved drugs fulfill two requirements:
• The drug must be found to be effective against the disease for which it is seeking approval.
• The drug must meet safety criteria by being subject to extensive animal and controlled human testing.
Gaining FDA approval usually takes several years to attain. Testing done on animals must be extensive and must include several species to help in the evaluation of both the effectiveness and toxicity of the drug. The dosage of any drug approved for use is intended to fall within a range in which the drug produces a therapeutic effect or desired outcome.
The safety and effectiveness of prescription drugs in the U.S. is regulated by the federal Prescription Drug Marketing Act of 1987. The Medicines and Healthcare products Regulatory Agency (MHRA) has a similar role in the UK.
The Mass Torts division represents numerous people in claims against companies that manufacture and/or market defective pharmaceuticals and/or medical devices. The substantial number of attorneys, staff and resources devoted to this division allows the firm to competently and conscientiously handle any group of cases, no matter how large, along with particular catastrophic injury cases.
What can I do?
If you or a loved one has suffered injury as the result of a pharmaceutical company, you may be entitled to compensation. For a free legal consultation, contact us today!