Our Services

We are the connection between you and your well-being.

At Life Medical Research Group, we are committed to advancing medical science and improving patient care through our comprehensive range of clinical research services. Our services are designed to support both participants and pharmaceutical sponsors throughout the research process. Here’s an overview of what we offer:

For Participants:

  • Clinical Trials and Studies: We conduct a diverse array of clinical trials in various therapeutic areas. By participating, you may gain access to cutting-edge treatments and contribute to the development of new therapies.

  • Pre-Screening and Eligibility Assessment: Our initial pre-screening process helps determine if you are eligible for a study. This involves a review of your health history and current condition to match you with the appropriate trial.

  • Comprehensive Medical Evaluation: Before enrolling, you will receive a thorough medical evaluation to ensure that the study is safe and suitable for you. This includes physical examinations, diagnostic tests, and consultations with our healthcare professionals.

  • Personalized Care and Monitoring: Throughout the study, you will receive personalized care from our dedicated team. We closely monitor your health and progress, providing regular check-ups and assessments to ensure your safety and comfort.

  • Access to New Treatments: Participating in a clinical trial can give you access to new and innovative treatments before they become widely available. This can be particularly valuable if you have a condition that has not responded to conventional therapies.

  • Compensation and Reimbursement: Depending on the study, you may receive compensation for your time and travel expenses. 

  • Confidentiality and Privacy: Your personal information and medical data are handled with the utmost confidentiality. We follow strict protocols to ensure that your privacy is protected throughout the study.

  • Education and Support: We provide educational resources about the study, including what to expect and how to prepare. Our team is always available to answer any questions or concerns you may have.

For Sponsors and CROs:

  • Study Feasibility and Site Selection: We conduct detailed feasibility assessments to determine the suitability of our site for your study. Our site is equipped to handle a variety of therapeutic areas and study requirements.
  • Participant Recruitment and Enrollment: Utilizing our extensive patient database and recruitment strategies, we facilitate effective participant recruitment and ensure timely enrollment to meet study goals.
  • Site Management and Coordination: Our experienced site team manages all aspects of site operations, including site initiation, monitoring, and close-out, ensuring seamless coordination throughout the study.
  • Data Collection and Management: We provide robust data collection and management services, including real-time data entry, validation, and secure storage, to ensure data integrity and compliance.
  • Regulatory and Compliance Oversight: Our site adheres to all regulatory requirements and Good Clinical Practice (GCP) guidelines, maintaining rigorous oversight to ensure compliance and ethical conduct.
  • Study Documentation and Reporting: We handle all study documentation, including regulatory submissions and progress reports, ensuring that all required information is accurately documented and submitted.
  • Quality Assurance: We implement strict quality control measures to maintain the highest standards of research conduct, data accuracy, and participant safety.

Who can participate

Our clinical research studies cover a range of therapeutic areas, each with its own specific eligibility criteria. You may qualify for one or more of our studies based on your health status and medical history. If you are interested in participating, we encourage you to contact us to learn more about the studies and determine your eligibility. Our team is here to help you find out if you meet the criteria for any of our ongoing or upcoming research projects.

Contact Us

NATIVE3:

NASH Trial

 

We are currently enrolling participants aged 18 and older for a Phase III clinical trial focused on Nonalcoholic Steatohepatitis (NASH). This study aims to evaluate the safety and effectiveness of an investigational treatment for individuals diagnosed with NASH. Qualified participants will receive study-related care and monitoring from experienced medical professionals at no cost.

 

 

SYNCHRONY HISTOLOGY:

NASH/ MASH Trial

 

We are currently enrolling participants from 18 to 80 years old for a Phase III clinical trial focused on Nonalcoholic Steatohepatitis (NASH/MASH). This study aims to evaluate the safety and effectiveness of an investigational treatment for individuals diagnosed with NASH. Qualified participants will receive study-related care and monitoring from experienced medical professionals at no cost.

 

 

SYNCHRONY OUTCOMES:

Compensated Cirrhosis due to NASH/ MASH Trial

 

We are currently enrolling participants from 18 to 80 years old for a Phase III clinical trial focused on compensated cirrhosis due to Nonalcoholic Steatohepatitis (NASH/MASH). This study aims to evaluate the safety and effectiveness of an investigational treatment for individuals diagnosed with NASH and compensated cirrhosis. Qualified participants will receive study-related care and monitoring from experienced medical professionals at no cost.

 

 

Sjögren's Syndrome Trial

 

We are currently enrolling female participants from 18 to 75 years old for a Phase II clinical trial focused on Sjögren's syndrome. This study aims at improving moderate to severe symptoms of fatigue, dryness and/or pain related to this disease. Qualified participants will receive study-related care and monitoring from experienced medical professionals at no cost.