Number of international outreach efforts during the month
Dictionary: Many medical products are being developed, manufactured, and sold throughout the world. Current regulatory requirements vary from country to country. OSMP has an important role in educating stakeholders internationally about US regulatory requirements to expedite the review and the availability of medical products in the US. OSMP staff attends international conferences and collaborates with international regulatory counterparts to promote such education and explore opportunities for harmonizing regulatory requirements for medical products.
Information is current as of December 31, 2012.
Fiscal Year - 2012
FY 2012 YTD: 70
Note: The data provided on this website is produced on an ongoing basis for performance management purposes and is subject to change due to updates of preliminary estimates, corrections, or other reasons. In addition, FDA may change the type or amount of data provided on this website at any time. Information marked as "Completed" may include measures and/or key projects for which activities are ongoing but no longer tracked as part of FDA-TRACK.