Boji Medical Technology Co., Ltd Boji Medical Technology Co., Ltd
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Services and Solutions

Clinical Research Services

SMO On-site Management

Shanghai Farmar Pharmaceutical Biotechnology Co., Ltd.specializes in end-to-end SMO services for clinical research, with in-depth expertise in oncology, endocrinology, respiratory diseases and other therapeutic areas, and is committed to building a high-end platform for biopharmaceutical R&D services.
SMO On-site Management
Clinical Research Services Pre-Clinical Research TCM FC-RS Therapeutic Areas Global New Drug Development Services Ongoing Project Transfer
Clinical Trial Operation Clinical Trial Operation

Clinical Trial Operation
Medical Writing Medical Writing

Medical Writing
Data Services Data Services

Data Services
CGT-Specific Clinical Research CGT-Specific Clinical Research

CGT-Specific Clinical Research
SMO On-site Management SMO On-site Management

SMO On-site Management
Medical Devices Medical Devices

Medical Devices
Clinical Bioanalysis Clinical Bioanalysis

Clinical Bioanalysis
Clinical Pharmacology Clinical Pharmacology

Clinical Pharmacology
Pharmacovigilance Pharmacovigilance

Pharmacovigilance
INTRODUCTION

INTRODUCTION

Shanghai Farmar Pharmaceutical Biotechnology Co., Ltd, a subsidiary of Boji Medical Technology Co., Ltd., focuses on providing clinical research site management services (SMO) for the R&D of innovative drugs (devices).The company's business spans the entire cycle of clinical research. It has rich clinical trial experience in fields such as oncology, endocrinology, respiratory system, rheumatoid immunity, digestive diseases, and pediatrics.

Farmar adheres to the belief that “quality is life”, takes service as the tenet, and promotes development with quality. It is committed to building a high-end platform for biomedical R&D services and safeguarding the health of the public.

OUR SCALE

  • Covered clinical trial sites
    1100+

    Covered clinical trial sites

  • Team scale
    350+

    Team scale

  • Covered clinical trial institutions
    300+

    Covered clinical trial institutions

  • Covered cities
    50+

    Covered cities

OUR ADVANTAGES

Efficient Launch Services
Efficient Launch Services
  • Efficiently empower pre-project training, center feasibility research and evaluation, center contracts, ethics document submission, research center contract tracking & progress follow-up, and implement proactive pre-operation monitoring.
High-Quality & Targeted Project Enrollment Advancement
High-Quality & Targeted Project Enrollment Advancement
  • Establish effective incentive mechanisms to efficiently drive project enrollment; update the investigator database in real time to precisely match project needs.
Clinical Trial Institution Filing & Medical Affairs Support Services
Clinical Trial Institution Filing & Medical Affairs Support Services
  • The only CRO in China that provides consulting services for clinical trial institution filing and medical affairs support.
Comprehensive Quality Management & Control
Comprehensive Quality Management & Control
  • Referencing the ISO9001 quality management system, we establish SOPs and relevant specifications (and continuously update and improve them). We integrate a sound CAPA management system throughout the entire clinical research cycle to ensure study quality.
Efficient Launch Services
Efficient Launch Services
  • Efficiently enable pre-project training, center feasibility research and evaluation, center initiation, ethics document submission, research center contract drafting/submission and progress follow-up, and implement proactive pre-operation monitoring.

SERVICE CONTENT

SSU Management
SSU Management
  • Selection of research units and recommendation of investigators
  • Feasibility research for clinical trials
  • Support for clinical trial project initiation
  • Preparation and submission support for clinical trial ethics review
  • Support for clinical trial contract processing
Subject Recruitment
Subject Recruitment
  • Develop a recruitment plan based on project requirements
  • Match project needs quickly by sorting and refining data with trial subjects as the core
  • Establish a priority site subject list based on hospital-end resources
Research Center On-Site Management
Research Center On-Site Management
  • Research center activation support
  • Coordinate subject pre-screening, screening and enrollment
  • Subject management
  • Research center document and source data management
  • Data entry, query and follow-up management
  • Management of drugs and biological samples
  • Assist in adverse event management
  • Internal quality control support
  • Support for various inspection coordination
  • Research center close-out support

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