The in-house team of biostatisticians and statistical programmers at Clinpacific life science solutions in the Asian region provides precise, high-quality, and timely biostatistics services. Practice findings, which is crucial for ensuring research success.

The team offers a robust statistical framework that translates scientific insights into clinical biostatisticians at  Clinpacific life science solutions have vast experience in providing biostatistics services across a wide range of therapeutic areas, from first-in-man to Phase IV trials. By working closely with other departments within Greenline Clinical Research, they ensure smooth integration and interpretation of statistical elements in the reporting and analysis of clinical data.

Clinpacifics life science solutions core biostatistics services include:

• Developing Statistical Analysis Plans (SAP)
• Managing and coordinating DSMB outputs and meetings
• Offering consultation on clinical trial design and protocols, including adaptive design studies
• Preparing Statistical Reports, including Interim, Final, and Clinical Study Reports
• Providing CDISC-compliant analysis datasets, such as SDTM and ADaM
• Offering support for randomization processes

core biostatistics services include:

1. Developing Statistical Analysis Plans (SAP)
2. Managing and coordinating DSMB outputs and meetings
3. Offering consultation on clinical trial design and protocols, including adaptive design studies
4. Preparing Statistical Reports, including Interim, Final, and Clinical Study Reports
5. Providing CDISC-compliant analysis datasets, such as SDTM and ADaM
6. Offering support for randomization processes

Clinpacific life science solutions utilizes high-quality, cost-effective strategies to ensure the successful management and delivery of clinical trial data. The primary objective in data management is to provide accurate, locked databases in an optimal format, delivered on time and within budget.

To accomplish this, Clinpacific life science solutions offers clients top industry tools for data management, including Medidata RAVE® and Greenline Trail Master® for eCRFs, ensuring a customized approach that aligns with each client’s needs, budget, and clinical site requirements.

The research data management services offered by CLINPACIFICS LIFE SCIENCE SOLUTIONS are adaptable to provide high-quality, cost-efficient solutions that meet the strictest regulatory standards.

Clinpacific life science solutions offers key clinical trials data management services that include:

• Design of Case Report Forms (CRF)
• CRF and data query tracking systems
• Data processing, including double data entry
• Coding of diagnoses, adverse events (AEs), and drugs
• Provision of CDISC ADaM-compliant analysis datasets
• Support for randomization processes

As clinical trial designs become more complex, the Asia region has solidified its position as a preferred hub for drug development. Biotech companies are now seeking more scalable solutions, particularly in terms of data quality and biometrics.

The Biometrics team has expanded to approximately 100 staff across Canada and North America, with a focus on retaining and nurturing top talent. This growth allows us to manage the full scope of biometric activities for global trials, not just regional studies. This capability provides significant advantages for clients aiming to leverage the benefits of various regions in their global trials.

Technology Solutions

Clinpacifics life science solutions Trial Master is a robust, cloud-based eClinical platform designed to enhance the efficiency of clinical trials. Since its launch in 2020, it has been utilized in over 100 trials across various therapeutic areas and clinical phases.

Developed by seasoned industry professionals, Clinpacifics life science solutions Trial Master merges innovative features with intuitive design to streamline your workflow. Our goal is to lead the way in eClinical innovation by creating smarter solutions that drive success for our client Clinpacifics life science solutions Trial Master adheres to all relevant regulatory standards, including ICH GCP, 21 CFR Part 11, and HIPAA.