Your organization spends a considerable amount of effort and resources on planning, authoring and distributing aggregate reports. Given the cross-functional nature of aggregate report authoring as well as global footprint of aggregate report distribution, it is easy to see how companies can lose oversight or create inefficiencies in their aggregate report process. Without a good handle on these operational complexities, there is a tremendous risk to experience a CAPA head ache after an inspection. Ever wonder what it would be like to go into an inspection confident that you knew the status of your aggregate reports?
See how one organization realized it needed to transcend the focus on aggregate report tracking to gain visibility of the whole landscape. This pharmacovigilance webinar will demonstrate proactive approaches to ensuring oversight of all aspects of the aggregate reports process and increasing compliance oversight in all areas of pharmacovigilance, leading to fewer and more effective CAPAs and improved health authority inspection readiness.
Please click here to register and join us for a free webinar on Thursday, October 12th at 12:00pm EDT.