By Julian Pecquet - 02/01/12 04:06 PM EST
• reducing total review times;
• meeting with companies if they miss a performance goal on an application and working out a plan to complete work on the submission;
• providing a "substantive interaction" with applicants halfway through the targeted time for completion of review to ensure they have time to properly respond to appropriate questions; and
• hiring an independent consulting organization to analyze FDA's management of the review process.
"The tentative new user fee agreement puts in place a framework that will benefit FDA and industry, but most importantly patients by accelerating the development and approval of safe and effective treatments and diagnostics," Stephen Ubl, president and CEO of the Advanced Medical Technology Association, said in a statement. "The improvements in the agreement provide FDA and medical technology companies the tools needed to improve the efficiency and consistency of the review process."
The FDA said it would develop a package of proposed recommendations for lawmakers to consider once final details of the agreement with industry are ironed out. The public will have a chance to comment on the recommendations before they are sent to Congress.