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OUR SERVICES


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REAL WORLD EVIDENCE



  • Comprehensive approach
  • Leverage real-world data (RWD) from electronic medical records (EMRs), administrative claims data, disease registries, and other health data repositories
  • Utilize databases like Flatiron, ConcertAI (Patient360 and RWD360), IQVIA Oncology EMR, Clinical Practice Research Datalink (CPRD), and Medical Data Vision (MDV)
  • Cover oncology indications like breast cancer, lung cancer, prostate cancer, gastrointestinal cancer, hematological cancer, and other non-oncology therapeutic areas
  • Global support for agencies and markets in United States, Italy, the United Kingdom, and Japan
  • External Control Arm studies (shows short-term priority evidence gaps, contextualizes long-term outcomes observed in clinical trials, and provides insights for health technology assessments and payer purposes)
  • Database studies
  • CDISC standardization
  • Implement CDISC standards for RWD to SDTM/ADaM conversion
  • Customized RWD analyses (customized treatment landscapes and in-depth biomarker)
  • Diverse range of stakeholders


ALL OUR SERVICES





BIOSTATISTICS



STATISTICAL PROGRAMMING



DATA MANAGEMENT



DATA MONITORING COMMITTEE (DMC)



REAL WORLD EVIDENCE (RWE)



MEDICAL AFFAIRS



MEDICAL WRITING



REGULATORY



CLINICAL OPERATIONS AND MANAGEMENT



OUR FLEXIBLE SERVICE MODEL





We can serve in roles as CRO that works on deliverable basis

  • Work in our office and on our system that is compatible with yours
  • Acquire services ‘as needed’
  • Significantly reduce your budgeting and management efforts
  • Provide fast response and quickly mobilize to assist with projects behind schedule
  • Advanced technology and tools that are compatible with your system


We can serve in roles equivalent to your external team

  • Work off-site on your system or our system that is compatible with yours
  • Can be your team members and work as FTE on the scopes with your assignment
  • You have direct access/manage our FTE resources
  • You are welcome to play a key role in the establishment of our study team
  • The study lead is employed by us, but has a solid line to your manager
  • You may utilize our expertise and knowledge (such as expert statisticians and expert programmers) beyond the assigned team members, if it is necessary

We provide the opportunity to harmonize standards and integrate into the sponsor’s system



ABOUT US





A growing CRO with a global footprint in U.S. and China


Building strategic partnerships or preferred vendor relationships with pharmaceutical companies, biotechnology companies and CROs


Flexible service models with experienced staff to deliver high quality products for your CSR, regulatory submission, or publication


Full commitment to excellence with our expertise, experience and passion to enable you to get to market faster, reducing time and cost



THERAPEUTIC AREA EXPERTISE





  • Oncology Immunology/Autoimmune
  • Rare Disease/Orphan Drug
  • Anti‐Inflammatory/Pain
  • Neurology/CNS
  • Cardiovascular
  • Gastroenterology
  • Ophthalmology
  • Allergy
  • Vaccine
  • Anti‐Infective
  • Diabetes & Metabolic Disease
  • Cell & Gene Therapy
  • Endocrinology
  • Infectious Disease/Vaccine


CONTACT INFO





Address: 220 Davidson Ave, Suite 201, Somerset, NJ 08873


Phone number: (908) 223-8823



Email: info@deltamedcro.com



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