https://caidya.com
Caidya | Clinical Research Organization | Contract Research Organization
Caidya formerly dMed Clinipace are a leading clinical research organization with a personal approach.
Caidya | Clinical Research Organization | Contract Research Organization News Events Careers Contact Us About Us Overview Invested in your success Mission, Purpose & Values Our mission & purpose Leadership & Expertise Meet Our Leadership Team Where we operate A CRO with global reach & patient access Our story so far Access for patients across the globe Corporate accountability DEI ESG Code of conduct Partners Vendor partners Become part of a trial Our Services Clinical Development Early phase development Phase II/III studies Clinical development expertise Clinical Operations & Delivery Study start-up Patient pathway & feasibility Regulatory Services & Surveillance Regulatory services Pharmacovigilance Medical writing Trial Data & Technology Biometrics and Biostatistics Clarity Clinical analytics Clinical data management Clinical technology and ecosystem RBQM Our Therapeutic Areas Cardiology Extensive experience in cardiovascular clinical trials Cell and Gene Therapy A personalized approach to CGT trials Gastroenterology Quicker startup, better outcomes Infectious diseases Experts in infectious disease studies Nephrology Developing strategies to successfully recruit and complete your study on time Neurology Neurology clinical trials Oncology Understanding the complexity of oncology studies Rare diseases Successful development, delivery and clinical approval for rare disease treatments Respiratory Exceptional knowledge, every step of the way Women’s health Transformative clinical research in women's health Submit RFP Overview Invested in your success Mission, Purpose & Values menu- column2 menu- column3 Who we are Overview Mission, purpose & values Leadership & expertise Where we operate Our story so far Corporate accountability DEI ESG Code of conduct Partners Investors Vendor partners What we do Overview Services Clinical Development Early phase development Phase II/III studies Clinical development expertise Clinical Operations & Delivery Study start-up Patient pathway & feasibility Regulatory Services & Surveillance Regulatory services Pharmacovigilance Medical writing Trial Data & Technology Biometrics and Biostatistics Clarity Clinical analytics Clinical data management Clinical technology and ecosystem RBQM Service models Therapeutic areas Cardiology Cell and Gene Therapy Gastroenterology Infectious diseases Nephrology Neurology Oncology Rare diseases Respiratory Women’s health Quality assurance Your journey Overview Become part of a trial Partner with us Careers Overview View open positions Being part of our team Contact Us Elevating your experience Clinical research built around you Caidya is a global, full-service CRO that activates the full potential of your science through our personalized partnership, global expertise and knowledge sharing. Partner with Us Trial transparency Your journey with Caidya 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. Your journey Harness the power of our industry-leading, cutting-edge clinical technology that integrates effortlessly to create an ecosystem that meets the specific needs of your study. Clarity synthesizes data from different systems within your technology ecosystem to create a near real-time view of your trial. This holistic view allows integrated teams within Caidya to transparently share information and data, generating insights to inform your decisions. Supporting you through every step of the clinical development journey Our approach puts you and your goals at the center of the project. We listen first, and then provide expert guidance to reach your goals. Our collaborative team is 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. Clinical research built around you 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. 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. Explore our service models 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. Oncology Rare diseases Neurology Infectious diseases Not what you are looking for? Explore all Oncology We understand oncology study intricacies: from the ever-changing regulatory landscape to novel and increasingly complex study designs to personalized treatment options. Learn more 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. Learn more Neurology We help activate the full potential of your scientific breakthroughs and overcome the challenges in CNS clinical trials with personalized services designed around the specific needs of your patients. Learn more 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. Learn more Not what you are looking for? Explore all Where we are Global reach, tailored approaches We can help you conduct successful regional, or multinational studies utilizing efficient operational models, local in-market expertise, and harmonized technologies. See our global reach Lingshi Tan, Ph.D. Executive Chairman of the Board John Scott, MBA Chief Information Officer Marie Hanley, BSN Senior Vice President, Global Quality Services Team & culture Our team and their vision We are liberating clinical research through listening for understanding, thinking openly, owning the success of each project we conduct, and sharing our knowledge every step of the way. Our people know their ideas, opinions, and contributions matter. We value transparency and integrity; supporting a collaborative and performance-oriented culture where everyone can thrive. Explore our mission Meet our leadership team Leading a new way The latest from Caidya Explore our news and updates as we liberate the clinical research process. Events 12th Annual Outsourcing in Clinical Trials Nordics 2024 1st October 2024 to 2nd October 2024 Copenhagen, Denmark View Event News 07/22/2024 Caidya Announces Leadership Transition: Barbara Lopez Kunz Named CEO Raleigh, N.C., July 22, 2024 – Caidya, a leading global... Read more Events 12th Annual Outsourcing in Clinical Trials Southern California 2024 24th September 2024 to 25th September 2024 San Diego, CA View Event [email protected] About Us Mission, purpose & values Leadership Where we operate Our story so far DEI ESG Code of conduct Investors Vendor partners Our Services Early phase development Phase II/III studies Clinical development expertise Study start-up Patient pathway & feasibility Regulatory services Pharmacovigilance Medical writing Biometrics and Biostatistics Clarity Clinical analytics Clinical data management Clinical technology and ecosystem RBQM Therapeutic areas Cardiology Cell and Gene Therapy Gastroenterology Infectious diseases Nephrology Neurology Oncology Rare diseases Respiratory Women’s health Your journey Become part of a trial Partner with us Careers View open positions Being part of our team © 2024 Caidya™. All Rights Reserved. Privacy Policy Transparency in Coverage CFIUS Disclosure Skip to toolbar Search
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