Product introduction

Clinical trials register

Product introduction: Provide medical, data management, statistical analysis services, follow international standard operating norms, and have experience in submission to mainstream regulatory agencies around the world, reduce research and development risks, accelerate the research and development process, and create multi-dimensional value for customers.

All-in-one solution empowered by professional medical, data management, and statistical analysis

All-in-one solution empowered by professional medical, data management, and statistical analysis

Real world study and post-marketing clinical study, including new indication study, investigator-initiated clinical research, and research required by regulatory authorities to evaluate drug efficacy and safety, etc. We provide professional services in medicine and data statistics, covering the design and writing of research plans, the construction of data collection platforms, data verification, and data statistical analysis, providing scientific evidence for safe and rational clinical usage of drugs.

One-stop solution empowered by professional medical, data management and statistical analysis

One-stop solution empowered by professional medical, data management and statistical analysis

By mining value from the data generated in the entire life cycle of drugs, we provide evidence for the transmission and communication of drug value, help companies successfully achieve market access, and accelerate market popularization.

Medical insurance, essential drugs and hospital access based on product value

Medical insurance, essential drugs and hospital access based on product value

Real world study and post-marketing clinical study

Pharma market access

标签模块(1)(1)(1)
Statistics
Medical Services
Real World Study
Digital Clinical Research
Health Economics Evidence

Statistics

Provide whole process data management and statistical analysis solutions

Data Management

Electronic data capture and management
Data management and data flow
   management
・Data collection and random system creation,  
   testing and maintenance

・Data management quality assurance and      
   auditing
・Medical Coding

Statistical Analysis

Research design and research protocol    
   development

・Develop templates for statistical analysis
   plans, tables, charts and lists
・Statistical analysis report
・Data monitoring committee

・Integrated Summary of Safety / Integrated
   Summary of Effectiveness
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Medical Services

Provide whole process standardized medical solutions

Medical Writing

・Clinical Protocol Writing

・Clinical Research Report Writing

・Medical Communication Materials Writing

・Medical Literature Research and Meta Analysis
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Real World Study

Dive into real world data,all-round support for R&D strategies, access strategies, academic research and market promotion of medicine and medical machinery

Real world study for clinical trials register

・Approved drugs are used to support  

  applications for expanded indications

・Real world study used for single-arm trial

・Real world study used to support drug  

  registration applications for rare disease

  treatments

・Hainan Lecheng exempts from clinical trials

  through real world study

RWD for post-marketing study

RWD used for post-marketing probative medical

   evidence

RWD used for pharmacoeconomic evidence

RWD used for treatment consensus guidelines  

   update

RWD used for patient flow analysis

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Digital Clinical Research

Make clinical research more convenient and efficient

・Provide digital clinical trial solutions ・Facilitate the digital transformation of enterprise clinical  trials
3Q digital clinical trial platform certification consulting service
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Comprehensive consideration of the value of medicinal equipment to facilitate

product market access

Health Economics Evidence

Health economics evidence as evidence of health care directory access

Health economics evidence as DRG/DIP Impact Analysis

Health economics evidence as evidence of essential drug selection

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Solutions

Our Advantages

Full lifecycle policy support

Complete and compliant data loop

Rich expert resources

Full lifecycle data management and analysis

National Medical Products Administration (NMPA)

National Health Commission (NHC)

National Healthcare Security Administration (NHSA)

Combining retrospective and prospective

Connecting Online and offline

Connecting inside and outside the hospital

Clinical and Pharmacy Specialist

Statistics and Epidemiology Specialist

Real World Research Specialist

Health Economics and Outcomes Research Specialist

Clinical trials register

Real world study and post-marketing clinical study

Health Economics research

Pharma market access Strategy Consulting

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Contact us

Tel:010-53681050

Contact e-mail:contact@medataccess.com

Contact address: Room209B, 2nd floor, Building No. 4,
                           Zhubang 2000 BusinessCenter,
                           No. 100 Balizhuangxili, Chaoyang District,Beijing
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International standards and quality as a benchmark

Provide customers with all-in-one solutions for the full lifecycle of pharmaceutical products