Need to demonstrate compliance in a hurry?
Post Market, Post Approval Studies
CRFweb is ideal for any post market (post approval) studies, but recent MDR and IVDR regulations for medical devices in Europe has upped the significance for that market in particular. If you want to market your medical device in Europe, you will need to meet compliance requirements, whether your appliance is new to market or already there. You will also need to provide ongoing evidence with respect to safety and efficacy.
CRFweb’s core attributes makes it the perfect option for post approval, post market research. Although capable of handling complex, lengthy trials, CRFweb’s super-fast, DIY set-up and simplicity of use, enables it to be put to a variety of uses. It’s ideal for putting together studies where turnaround time is of the essence and flexibility is paramount.
Our ePRO and eDIARY modules are of particular benefit to those looking at post market evaluation.
Whether your requirement is for post-marketing studies, registries, safety, observational or any other ongoing research for a product or service already in the marketplace, CRFweb can deliver a fast, efficient and bespoke solution. If you have an existing pre-market trial software system, it may well not meet your needs for post-market research. If you’re paper-based, A post-approval study can be the ideal first step into clinical trial software. Meet your regulatory and/or marketing requirements.. for a much lower outlay than you might imagine.
Contact us today to arrange a web demo and see how we can assist your post market evaluations.
While suitable for any post market studies, recent MDR and IVDR regulations in Europe has upped the significance for medical devices in particular. If you want to market your medical device in Europe, you will need to meet compliance requirements, whether your appliance is new to market or already there. You will also need to provide ongoing evidence with respect to safety and efficacy.
CRFweb’s core attributes makes it the perfect option for post-approval, post-market research. Although capable of handling complex, lengthy trials, CRFweb’s super-fast, DIY set-up and simplicity of use, enables it to be put to a variety of uses. It’s ideal for putting together studies where turnaround time is of the essence and flexibility is paramount.
Our ePRO and eDIARY modules are of particular benefit to those looking at post market evaluation.
Whether your requirement is for post-marketing studies, registries, safety, observational or any other ongoing research for a product or service already in the marketplace, CRFweb can deliver a fast, efficient and bespoke solution. If you have an existing pre-market trial software system, it may well not meet your needs for post-market research. If you’re paper-based, post-marketing can be the ideal first step into clinical trial software. Meet your regulatory and/or marketing requirements.. for a much lower outlay than you might imagine.
Contact us today to arrange a web demo and see how we can assist your post market evaluations.
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