Biotech Solutions with Specialist Biometrics Expertise

Accelerate Clinical Development With Tailored Support From Biotech Experts

Phastar specializes in delivering clinical trial services built around the needs of biotech companies. From study design and specialist biometrics support to regulatory insight and data visualization, our team works as an extension of yours to accelerate development while managing cost and risk.

Speak to our biotech specialists today

Why Biotech Trials Are Different

  • Fast-paced timelines to meet reach pivotal milestones
  • High regulatory scrutiny in emerging and complex therapeutic areas
  • Complex scientific requirements that demand flexible, scalable solutions
  • Cross-functional pressure to deliver across clinical, regulatory, and investor expectations

With the right specialist biometrics CRO partner, you can overcome complexity and build a solid foundation for growth.

How Phastar Supports Biotech Sponsors

Flexible models

From project-based services to functional sourcing

Expert teams

Biostatisticians, programmers, and data scientists with biotech experience

Regulatory insight

Support across submissions and agency interactions

End-to-end specialist biometrics and data science solutions

From design to submission-ready analysis

Discover how we scale with your program

Deep Therapeutic And Regulatory Knowledge

We support biotech sponsors working across multiple therapeutic areas such as:

  • Oncology
  • Rare diseases
  • Neurology
  • Cell and gene therapy
  • Infectious diseases and vaccines

Combined with our understanding of global and regional regulations, we help design and execute studies that are both scientifically robust and regulatory ready.

Data-Driven, Outcome-Focused

Data is at the heart of every clinical decision. Phastar brings a optimized tech-enabled, intelligence-led approach to trial delivery:

  • AI-powered analytics and simulation modeling
  • Real-time dashboards and data visualization
  • Risk-based quality monitoring and central oversight

From planning to submission, we use data to drive better decisions, faster.

Optimized Tools And Technologies

Our experts use proven platforms and in-house innovations to support biotech trials:

  • Integrated data capture and review systems
  • Collaborative trial management tools
  • Compliance-ready workflows aligned to ICH, GCP, and regulatory guidelines

We combine best practices with the right technology to deliver high-quality results without compromise.

Need expert help for your current or upcoming study?

Core Services For Biotech

Biostatistics, Programming, Data Management, and Data Science: Expert-led
trial design, analysis, and submission packages.

FSP Models: Agile biometrics support tailored to your pipeline needs.

Rescue Studies: Rapid intervention to turn around at-risk or delayed trials.

Explore More in these Featured Resources

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Articles & Interviews

Building Effective Partnerships Between Biotechs and CROS to Optimize Outsouring

April 22nd, 2025 1 minute read

With biotechs increasingly driving innovation in research and development, it is important for organizations to choos…

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Vendor Selection in Biotech Partnerships: Key Factors for Success

February 27th, 2025 4 minute read

Introduction  For biotechs looking to advance clinical development, selecting the right CRO partner can be a def…

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The Value of Strategic Collaboration: Overcoming Key Challenges in Biotech Development Through Effective Outsourcing

January 23rd, 2025 4 minute read

Introduction  In today’s fast-evolving environment, biotechs need to form strategic partnerships to address reso…

Understanding the Growth of Biotech in Clinical R&D and Its Need for Strategic CRO Partnerships
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Understanding the Growth of Biotech in Clinical R&D and Its Need for Strategic CRO Partnerships

January 16th, 2025 4 minute read

Introduction  The biotech industry has become a driving force in clinical research, accelerating advances in are…

Building Effective Partnerships Between Biotechs and CROs to Advance Clinical Development 
Publications

Building Effective Partnerships Between Biotechs and CROs to Advance Clinical Development 

September 26th, 2024 1 minute read

The biotech industry is evolving rapidly, with emerging companies leading the charge in clinical development. As outs…

Specialist CROs: The Strategic Partnership Needed for Biotechs
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Specialist CROs: The Strategic Partnership Needed for Biotechs

June 10th, 2025 1 minute read

In a recent Q&A with European Biopharmaceutical Review, Stephen Corson—Associate Director of Statistics and Techn…

Biotech Solutions FAQs

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We offer flexible engagement models that adapt to your needs, from full-service to on-demand biometrics support. Our teams are experienced in working with lean, fast-moving biotech sponsors.
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Yes. We provide statistical and programming support for regulatory submissions and can assist with documentation, analysis outputs, and agency interactions.
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Absolutely. These are core areas of expertise for our specialist teams, including experience with adaptive designs, small sample sizes, and accelerated pathways.
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Our rescue study services provide focused, rapid-response support to identify issues and stabilize delivery, without adding unnecessary delays.
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Yes. We work with widely used EDC and analytics platforms and can integrate our solutions into your existing workflows.
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Yes. Phastar operates globally with teams across North America, Europe, Asia and Africa allowing for regional insight and round-the-clock execution.

Ready to Empower Your Biotech Clinical Development?

Partner with Phastar for expert-led, scalable support tailored to your program’s needs.