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Phase II-IV Clinical Trial Management
Vast Therapeutic Expertise, Global Reach, and Seamless Execution
Lambda Therapeutic Research specializes in facilitating Phase II-IV studies for investigational new drugs (INDs), biologics, and medical devices. With over two decades of clinical operations experience, we offer a solid foundation and a comprehensive array of services to navigate the complexities of multi-centric clinical programs across various therapeutic areas. Our services encompass the entire clinical trial lifecycle, from initial study feasibility and pre-site qualification to study initiation, patient recruitment, site management, and thorough study monitoring, incorporating Central Monitoring, Remote Monitoring, and on-site monitoring.
Lambda & Novum has enrolled 85000+ patients in various therapeutic categories and conducted over 280 multicentric trials across different geographies with data submitted to all leading agencies including US FDA, EMEA, DCGI, ANVISA.
Therapeutic Expertise:
Lambda specializes in assisting small and mid-sized biotech Companies focused on groundbreaking science, particularly in intricate and challenging disease areas. Drawing upon extensive experience and proven expertise in these complex therapeutic domains, we bolster your team on the path to providing renewed hope for patients through the clinical journey. Our adept experts are enthusiastic about sharing their specialized knowledge and collaborating with you to drive forward your therapeutic pursuits.
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Patient-Based PK Studies
Accelerating patient-based PK studies across therapeutic areas with a proven track record, overcoming challenges with precision and innovation.
Our Experience
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Our Experience
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Experience the Lambda Advantage
Lambda’s Phase II-IV Clinical Trial Management services offer a blend of experience, global reach, and disciplined execution. We empower your clinical trials with tailored solutions, propelling your product towards successful commercialization while ensuring utmost safety and efficiency. Trust Lambda to manage your trials with expertise and precision, meeting your unique objectives at every stage of development.
Experts from various fields such as medicine, pharmacy, biotechnology, and life sciences, ensuring a comprehensive approach to clinical trial management.
Streamlining the entire process from inception to commercialization.
Extensive experience in managing multi-centric clinical trials spanning diverse therapeutic areas, ensuring a global perspective in study execution.
Leveraging our extensive global site alliance network, we ensure efficient trial conduct and data collection across various regions.
Strong expertise in New Drug Delivery Systems (NDDS) and biosimilars, adding a strategic edge to your clinical development.
Proven track record in handling complex molecules across a wide range of therapeutic areas, bringing valuable insights to your trials.
We utilize a sophisticated and fully customizable Clinical Trial Management System (CTMS), seamlessly integrating every facet of the trial process. This technology allows for real-time data access, efficient communication, and informed decision-making.
Let's Unveil New Therapies Together
Connect with our experts to leverage our proven track record of clinical research excellence.