Medwatch Form 3500. With only section d (suspect medical device). November 01, 2005 for use by health professionals and consumers for voluntary reporting of adverse.
Regulatory Submissions Product Documentation
Web medwatch consumer reporting form 3500. Form fda 3500 may also be used to submit reports about tobacco products and dietary supplements. See pra statement on page 5. Ad download or email fda 3500a & more fillable forms, register and subscribe now! 06/30/2025 (see pra statement below) when do i use this form? Web form fda 3500 may be used to report to the agency adverse events, product problems, product use errors, and therapeutic failures. With only section d (suspect medical device). Medwatch form is specially designed by mastercontrol to cater medical device reporting requirements. Triage unit sequence # fda rec. Department of health and human services food and drug administration.
Web mail or fax the form to: For the device that is most likely to have caused or contributed to the event and a separate. When do i use this form? Web medwatch is the fda reporting system for adverse events (aes), and form 3500a is used for adverse event reporting. Web mail or fax the form to: Web an approved application. Web (form fda 3500b) form approved: Web medwatch consumer reporting form 3500. Web instructions for completing form fda 3500. November 01, 2005 for use by health professionals and consumers for voluntary reporting of adverse. There are two types of medwatch forms:.
