PDG offers one-stop-shopping to include 513(g) requests for information, pre-submission meetings (formerly pre-IDE meetings), IDE filing and Institutional Review Board (IRB) approvals, 510(k) and PMA submissions. Our expertise includes, clinical development in parallel with strategic regulatory planning and manufacturing and other third party vendor audits. Call : 08133332950 Email : info@pharmdevgroup.com Visit : https://pharmdevgroup.com/medical-device-consulting/