Access a global team of trusted experts
At Phastar, we have over 400 technical experts across 11 countries , with experience across the full spectrum of biometrics, from strategic consulting to regulatory strategy. Through collaboration and building robust partnerships, we’re able to create flexible and dynamic solutions to your specific challenges.
Our customer-centric approach puts you at the heart of solution delivery. We’ll take the time to explore your clinical development and outsourcing objectives. Then we’ll craft a bespoke strategy that meets your specific needs, including levels of oversight, risk tolerance and insourced (Functional Service Provision) or outsourced (Project Based Services) staff. Talent will be sourced from across Phastar to deliver the strategy with optimal efficiency and ultra-high performance, all mapped to your functional requirements.
We can even adapt delivery to your needs throughout the project, ramping up support at key moments to help ensure you hit your submission targets.
We specialize in supporting Biotechs throughout the drug development journey. We can work with you from the very start, helping you meet each critical milestone. We’ll be a central point of contact for all stakeholders, support with navigating regulatory constraints and ensure every deliverable is of the highest quality. Flexible delivery approaches and access to a tailored suite of advanced analytics tools mitigate risk and create cost-efficiencies throughout the project lifecycle. As strategic partners and therapeutic experts, we’re committed to accelerating your drug development program forward to a successful outcome.
At Phastar, we have in-house specialists across the full spectrum of biometrics. Our expertise spans from planning and design to data management and analytics, tailored precisely to meet your requirements. We’re flexible to your needs, whether it’s engaging one consultant or assembling a project team from inception to submission. Each consultant excels in their domain, actively contributing to pioneering research and innovation, ensuring direct application of the latest insights to your project.
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Our statistical consultants are at the forefront of innovation. Through our work, we identify novel concepts and methodologies for investigation, partnering with leading academic institutions to publish findings in peer-reviewed journals. We then take these insights directly into your projects, ensuring you’re always getting the latest advice and expertise for your clinical trial.
Poor regulatory quality can significantly impact study timelines, submissions and ultimately commercialization. At Phastar, we’re proud to say that we’ve never had a trial rescued. In fact, we’re the go-to CRO for trial rescues.
If your trial is at risk of missing the deadline or if the quality is in doubt, we can help. We’ll evaluate the extent and nature of the issues, identifying all necessary remedial actions. Then we’ll step in as a third-party entity and assist in overseeing the project.
We’ll provide guidance to your project team, coordinate with third party CROs and even take full responsibility for managing your study. Our extensive global experience, understanding of local regulatory frameworks and suite of advanced technologies mean we can act quickly and efficiently to put your trial back on the PHAStrack to approval.
We leverage our extensive expertise in health data domains and cutting-edge technology to assist you in acquiring valuable insights and actionable data from your datasets.
Our broad experience encompasses an array of services, including comprehensive end-to- end data solutions and the identification of unmet medical needs. We merge diverse skill sets in design and critical analysis to aid you in exploring historical data or evidence from real-world scenarios, identifying undiagnosed patients, and crafting remote/virtual access to patient data.
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Unlock the full potential of digital health for your trial.
There any many clinical trial methodologies. Some are based on well-established fixed models, while others require complex strategies and novel methodologies to achieve the intended efficiencies. Our in-house experts specialize in two key efficiency driven flexible models, Adaptive and Bayesian design. We have extensive experience planning, creating and running studies using these methodologies at every stage of a clinical trial, from planning and simulation/elicitation to delivery and analysis. We can support you end-to-end, applying precision and scientific rigor to help you realize meaningful efficiencies and successful regulatory outcomes.
Speak to one of our experts for advice on utilizing adaptive and Bayesian methods in your trial.
We understand every step required to create a submission-ready regulatory package. Our team can work within your systems or assemble a dedicated project team, creating all the relevant documentation to the highest quality standards. We adhere to our Phastar Discipline, a framework of rules designed to create error-free work, in addition to our unique three-stage quality check process. Giving you the confidence that your clinical trial is being developed with regulatory integrity.
Our team of Statistical Consultants and Data Scientists are at the forefront of the biometrics industry. See the latest articles from our specialist team.
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