Clinical Trial Management Support
Ensuring quality and performance throughout study start-up activities is a crucial part of a successful clinical trial. At BPX, we have the experience and expertise to help you avoid the usual pitfalls every step of the way – from pre-study screenings and visits to vendor selection and set up to study execution and study rescue. Our team will work with you to ensure that your clinical research is conducted smoothly and efficiently, resulting in a higher quality clinical trial. With our help, you can be confident that your study will be kick-started and executed with excellence, giving you the best chance for success.
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What We Offer
BPX offers a range of clinical trial support services to pharmaceutical and biotech companies, including: managing CROs and vendors, vendor selection, site evaluation, informed consent design, essential document review, performing Virtual Initiation Visits, regulatory document collection and storage within designated CTMS, and more. Our team has the experience and expertise to help you avoid the usual pitfalls every step of the way – from pre-study screenings and visits to study execution and study rescue. With our help, you can be confident that your study will be kickstarted and executed with excellence, giving you the best chance for success. From regulatory consulting to clinical operations management, we have the experience and expertise to help you succeed in your clinical trials from the start or in a mid-stream study rescue.
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What Makes Us Different
BPX offers a range of clinical trial support services to pharmaceutical and biotech companies, including: managing CROs and vendors, vendor selection, site evaluation, informed consent design, essential document review, performing Virtual Initiation Visits, regulatory document collection and storage within designated CTMS, and more. Our team has the experience and expertise to help you avoid the usual pitfalls every step of the way – from pre-study screenings and visits to study execution and study rescue. With our help, you can be confident that your study will be kickstarted and executed with excellence, giving you the best chance for success. From regulatory consulting to clinical operations management, we have the experience and expertise to help you succeed in your clinical trials from the start or in a mid-stream study rescue.
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How We Deliver
At BPX, we understand that at companies large and small, it can be difficult to manage CROs, who often overpromise and underperform, leading to multiple change orders, delays in timelines, protocol deviations and poor quality. To address this, we work to anticipate gaps, mitigate risks to ensure realistic expectations, high quality and excellence in performance. We partner with you to oversee CRO performance, minimize change orders and delays in timelines.
We know that time is precious, so we make sure to do all the hard work for you. We'll scour the market and compare CROs so that you can be sure you're getting the best possible deal. And because we believe in transparency, we'll always keep you updated on our progress.