Devicemakers Still Leery of Using Third-Party Inspection Program

Devicemakers have not shown much interest in the FDA’s third-party accredited persons program, but the agency isn’t giving up on the idea yet, Larry Spears, deputy director for regulatory affairs at CDRH, said last month at FDAnews’ Fourth Annual FDA Inspections Summit. “We need to get more participation on the part of industry. We haven’t really seen much change yet,” he said.
The GMP Letter