Clinical development journey

We offer a uniquely personalized approach. Our experts are collaborative and focused on activating and sharing knowledge and expertise with you, every step of the way, from pre-IND strategy, through clinical development to submission and post-marketing surveillance.

Global, personalized clinical research solutions

Supporting you through every step of the journey

Caidya activates the full potential of your science through our personalized partnership, global expertise and knowledge sharing.

Regulatory Strategy

Across a wide range of therapeutic areas, we develop regulatory strategies to help you most efficiently navigate complex processes and advance your program into the clinic and beyond.

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Clinical Development

Experts help shape a personalized solution, getting involved in the earliest stages of your project to understand and map requirements and develop a tailored strategy for your clinical program.

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Project Management

A highly skilled team of research professionals and clinicians drive the project management and all functions for your clinical trials, always with an ownership mindset where we treat your project like our own.

Patient Pathway & Feasibility

We improve patient recruitment and retention in your trial by thoroughly understanding patient pathways, determining optimal study site profiles and validating protocols that reduce patient and caregiver burdens.

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Study Start-up

Identify and enroll patients, prepare and train study sites to accelerate your development time and create the foundations for success.

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Data Management

You get a best-in-class solution for your study combining the latest technologies with knowledge and expertise to identify and resolve data discrepancies, identify trends, and ensure the highest data quality.

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Biometrics/Biostatistics

Monitoring and reporting your clinical data with a hands-on approach means you can make the right decisions at the right time in your project.

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Clinical Analytics

Expert analysis to inform decisions and help you maximize your trial data for any phase, in any therapeutic area, around the world.

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Medical Affairs

Monitoring patient safety on an ongoing basis to ensure the progress of your clinical trials, minimizing protocol deviations and ensuring the highest possible data quality.

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Pharmacovigilance

Managing adverse events and supporting the submission of expedited and periodic reports from clinical trial drug safety to post-marketing safety surveillance.

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Medical Writing

Sharing knowledge and experience in a wide range of global clinical research guidelines to tell your product’s story and help realize the full potential of your science.

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Quality Assurance

Meeting regulatory standards and navigating through changing demands of studies while ensuring the integrity and safety of your trial to ICH GCP standards.

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RBQM

Proactively identifying, tracking and mitigating risk and using statistics to remove extraneous differences between sites and perform a holistic review for risk signals in integrated trial data.

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Clarity

Synthesizing data from different systems within your technology ecosystem to create a complete, near real-time view of your trial, generate insights, and inform your decisions, every step of the way.

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Exceptional personalized experiences

Full-service support combined with vast therapeutic expertise

Our clinical research services connect you with unrivaled access to specialist knowledge and personalized solutions on a global and local scale that remove barriers to enable better healthcare outcomes for all.

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Our clinical research services

From a single service project to portfolio-level integrated services, we offer custom, scalable approaches that get you the right resources in the right seat, when and where you need them.

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Therapeutic area expertise

We have the depth and breadth of therapeutic and global market expertise you need, coupled with the flexibility you’ve been looking for to give your therapy the best opportunity to get to patients in need.

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Oncology

We understand oncology study intricacies: from the ever-changing regulatory landscape to novel and increasingly complex study designs to personalized treatment options.

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Rare diseases

We understand the unique challenges in performing rare disease trials and can guide you in the strategy, design and implementation of trials involving smaller patient numbers.

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Nephrology

Led by scientific experts, our team understands the nuances of your nephrology studies in both rare and non-rare indications.

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Infectious diseases

Select the right place and patients for your clinical research into infectious diseases with a partner closely aligned with and experienced in your therapeutic area.

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Gateway to the globe

Speak to a global expert

Access to the right people when and where you need them with personalized clinical services tailored to your and your trial.

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Leading a new way

The latest from Caidya

Explore our news and updates as we liberate the clinical research process.

News

10/03/22

dMed | Clinipace announce corporate name change to Caidya

SHANGHAI and MORRISVILLE, N.C., October 3, 2022 – dMed | Clinipace, ...

News

04/28/21

CROs dMed and Clinipace merge to accelerate customer success

SHANGHAI, CHINA and MORRISVILLE, NORTH CAROLINA, USA, April 28, 2021 – ...