Featured Articles
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                    The Gig Economy And GxP Auditing In 2024
                        11/2/2023
                    See how this unique GxP auditing approach can ensure that vendors are complying with all rules and regulations quickly and efficiently, benefiting sponsors and auditors alike. 
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                    3 Enrollment Barriers And How To Overcome Them
                        11/2/2023
                    Read along as this author sheds light on the top three common barriers to clinical trial enrollment and offers a fundamental framework for overcoming these challenges. 
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                    Selecting The Right Pharmacovigilance Vendor
                        10/3/2023
                    Delve into several key benefits of entrusting pharmacovigilance needs to a qualified vendor, from economic efficiency and access to expertise to ensuring regulatory compliance and patient safety, and more. 
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                    Building Strong Relationships With Patient Advocacy Organizations
                        10/3/2023
                    When engaged with, patient advocacy organizations can be an invaluable resource. Delve into various strategies for establishing trust and long-lasting relationships with PAOs. 
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                    3 Simple Tips for Preventing Clinical Trial Fraud
                        9/6/2023
                    Clinical trial fraud is a prevalent issue that demands attention. Review several strategies for upholding due diligence and substantially reducing the risk of fraud in clinical trials. 
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                    5 Benefits Of Outsourcing Your Next Study To 2 CROs
                        8/31/2023
                    Examine the merits associated with the strategic pairing of two distinct contract resource organizations: one focused on clinical requirements and the other specialized in biometrics. 
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                    How To Evaluate & Select The Right eQMS For Your Needs
                        7/17/2023
                    Learn how partnering with an experienced functional service provider can help evaluate, implement, and integrate a QMS system while allowing core teams to stay on task. 
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                    Clinical Research Safety: Ensuring Participant Protections
                        7/17/2023
                    Gain a better understanding of how trials are designed and carried out with patient safety at the top of mind. 
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                    Understanding When And How To Terminate Your CRO
                        7/17/2023
                    Ever think about terminating your CRO contract? Delve into the reasons why you might, the potential implications, and the strategies for a successful exit and transition process. 
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                    FDA Releases Updated Draft Guidance On Decentralized Clinical Trials
                        6/12/2023
                    Take a closer look at the FDA's draft guidance on designing and implementing DCTs, notably remote trial visits, the use of digital health technologies, institutional review board oversight, and more. 
