MedWatch Form

MedWatch Form is Specially Designed by MasterControl to Cater Medical Device Reporting requirements

There are two types of MedWatch forms: MedWatch Form 3500 and MedWatch Form 3500A. MedWatch Form 3500 represents a voluntary reporting form and should be used by consumers, healthcare professionals and patients to report serious adverse events. As stated by the FDA serious adverse events would be events related to "human medical products, including potential and actual product use errors, product quality problems, and therapeutic inequivalence/failure."

MasterControl eMDR™
Download