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.
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.
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.
When engaged with, patient advocacy organizations can be an invaluable resource. Delve into various strategies for establishing trust and long-lasting relationships with PAOs.
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.
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.
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.
Gain a better understanding of how trials are designed and carried out with patient safety at the top of mind.
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.
Take a closer look at the FDA's draft guidance on designing and implementing DCTs, notably remote trial visits, the use of digital health technologies, institutional review board oversight, and more.
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