Study monitoring is a resource intensive proposition. Finding, training and managing the CRAs needed to effectively monitor clinical studies to maintain compliance is both time consuming and expensive, especially when hiring these types of professionals into your organization.
We will work with your clinical leads to scope a right-sized solution for your clinical study by ensuring appropriate resources are effectively deployed, to maintain compliance and data integrity.
Our accredited team of monitors have a deep knowledge of clinical studies and the mandatory regulations to ensure your success.
We view our monitors as part of your clinical team, giving your sites a seamlessly integrated impression of your organization.
AlvaMed effectively conducted the IDE study, performed study data cleaning, closure, issued the final study report after meeting the client’s enrollment needs, and received De Novo clearance for the client’s device based on final IDE study report data.
The AlvaMed Team played a pivotal role in our early success and the achievement of our key milestone – our First-In-Human clinical experience. Their unwavering support and expertise were instrumental in navigating challenges and driving us forward. We highly recommend AlvaMed as a dedicated and invaluable partner committed to turning visions into reality.
CEO, Co-Founder, Eclipse Regenesis, Inc
I just wanted to say thanks again for all of the hard (and high quality) work that you’ve done to support BFKW but most recently, getting the BFKW India trial up and running. It seems like it’s been “crunch time” for a while now but the team has pulled it off with the recent formal opening of enrollment.
BFKW, LLC
Mark and his group have consistently provided exceptional deliverables in a timely and cost effective manner.
MedTech Client
AlvaMed effectively conducted the post-market study and is in the close-out process after meeting the client’s enrollment needs.
CASE STUDY
While many of our clients choose to utilize our full suite of CRO services, we do offer stand-alone Clinical Monitoring.
Yes. Our monitors have experience both on site and working through remote access to satisfy the needs of your monitoring plan.
Our monitors have accreditations from SOCRA, CCRA, and others agencies.
At AlvaMed we have a deep pool of CRAs, with extensive knowledge of clinical trials and therapeutic area expertise. We can help you outsource this expensive endeavor, saving you time, cash-burn and headcount expenses, all while delivering highly skilled, experienced clinical professionals, who can integrate seamlessly into your organization, like they were one of your own.
Schedule a meeting with Marc to discuss how AlvaMed can help with clinical study monitoring.
