With FDA approval, their ground-breaking new drug could be made available to thousands of asthma sufferers across the United States; this, in turn, would generate millions of dollars in revenue that would fund additional research.However, because client’s master batch records were written in French, the partners found themselves with over 500 pages of documentation that needed to be translated in order to submit the treatment to the FDA for approval. And due to the pharmaceutical industry’s stringent regulations that require superior translation services employing consistent, accurate terminology, the translation process promised to be complex.