Clinical Trial Management
Clinical Trial Management
Clinical Trial Management
Integrated Clinical Development Services
We offer both on-site and remote monitoring services tailored to the specific needs of your study, ensuring flexibility and cost-efficiency.
We offer both on-site and remote monitoring services tailored to the specific needs of your study, ensuring flexibility and cost-efficiency.
We offer both on-site and remote monitoring services tailored to the specific needs of your study, ensuring flexibility and cost-efficiency.
On-site and Remote Clinical Monitoring Services
We offer both on-site clinical monitoring and remote monitoring services, tailored to the specific needs of your study, ensuring flexibility and cost-efficiency.
On-site and Remote Clinical Monitoring Services
On-site and Remote Clinical Monitoring Services
We offer both on-site clinical monitoring and remote monitoring services, tailored to the specific needs of your study, ensuring flexibility and cost-efficiency.
Risk-Based Monitoring (RBM)
Our monitors implement risk-based monitoring in clinical trials, focusing on high-risk areas of a study, optimising resources while maintaining data quality.
Risk-Based Monitoring (RBM)
Risk-Based Monitoring (RBM)
Our monitors implement risk-based monitoring in clinical trials, focusing on high-risk areas of a study, optimising resources while maintaining data quality.
Oversight Monitoring
Micron offers oversight of all services employed in the development of your product, including other CROs.
Oversight Monitoring
Oversight Monitoring
Micron offers oversight of all services employed in the development of your product, including other CROs.
Regulatory Compliance
With in-depth knowledge of ICH-GCP guidelines and evolving global regulatory requirements, our team ensures end-to-end regulatory compliance in clinical trials. We are adept at gaining the speediest approval from health authorities for your study to proceed.
Regulatory Compliance
Regulatory Compliance
With in-depth knowledge of ICH-GCP guidelines and evolving global regulatory requirements, our team ensures end-to-end regulatory compliance in clinical trials. We are adept at gaining the speediest approval from health authorities for your study to proceed.
Patient Safety and Data Integrity
Patient safety and data integrity are our highest priority. We ensure your trial meets the strictest standards for patient risk mitigation while safeguarding clinical data accuracy and regulatory readiness for submission.
Patient Safety and Data Integrity
Patient Safety and Data Integrity
Patient safety and data integrity are our highest priority. We ensure your trial meets the strictest standards for patient risk mitigation while safeguarding clinical data accuracy and regulatory readiness for submission.
Therapeutic Area Expertise
Our clinical research professionals have expertise across multiple therapeutic areas, ensuring that monitoring is conducted with a full understanding of the clinical and scientific context. Our focus is primarily infectious diseases, oncology and immunology, but we have also worked in many other areas.
Therapeutic Area Expertise
Therapeutic Area Expertise
Our clinical research professionals have expertise across multiple therapeutic areas, ensuring that monitoring is conducted with a full understanding of the clinical and scientific context. Our focus is primarily infectious diseases, oncology and immunology, but we have also worked in many other areas.
Have a project for us?
We would like to hear from you.
Have a project for us?
We would like to hear from you.
Have a project for us?
We would like to hear from you.
Have a project for us?
We would like to hear from you.
Integrated Clinical Development