Pharmalink Healthcare

Biometrics

• Pharmalink leverages cutting-edge advancements in data analysis and visualization to enhance clinical experiences. Our comprehensive, results-driven services in Biostatistics and SAS Programming are delivered by a knowledgeable team that collaborates closely with sponsors and functional areas to enhance quality, reduce timelines, and support the execution of your specific trial, enabling better data-driven decisions sooner. With over two decades of experience in clinical trials, we provide expert guidance in adaptive designs and integrated analyses, helping clients reduce time to regulatory submission and market approval.

Clinical Monitoring

• The best patient care is achieved with a consistent approach and staff. Our CRAs create the foundation for a stable and controlled clinical trial. With an average of 12 years of experience, our seasoned employees are aligned with the latest industry tools and intelligence.

Feasibility

• Pharmalink develops local relationships with patients and healthcare professionals globally. Our full-service CRO has representation across all states in India to meet immediate demands. We determine optimal locations for clinical trials using valuable data from our industry experience.

eTMF & Document Management TMF Services & Support

• Pharmalink offers both long-term and short-term solutions for TMF and Document Management Support. Working with our experienced team ensures effective management of TMFs for your clinical trial, in addition to supporting various other activities. Our flexibility allows us to operate within multiple systems to accommodate your specific needs, ensuring operational efficiencies using the most modern, cloud-based, and integrated solutions.

Medical Services

• Pharmalink provides comprehensive medical services and patient safety management throughout all stages of development. Our medical directors and safety experts are involved in daily clinical monitoring and safety activities, as well as all pre- and post-study procedures, from study design and protocol development to the preparation of your Clinical Study Report (CSR).

Medical Writing

• Our Medical Writing team excels in preparing protocols, CSRs, and various other clinical reports and articles. Working in close collaboration with functional experts, including the Medical Monitor, our Medical Writers ensure accurate and precise deliverables, with each version of the CSR undergoing rigorous internal QA for exact, high-quality documentation.

Quality & Validation

• Compliance is critical in clinical trials. Pharmalink’s Clinical Quality Services guide clients through global regulatory changes, helping them avoid fines and delays due to non-compliance. Our support allows industry professionals and project managers to optimize their time and focus on essential clinical and production tasks within the Medical Device, Pharmaceutical, and Biotech Industries.

Project Management

• Our Project Managers specialize in team management, forecasting, work breakdown structures, tracking and analysis, and other key performance indices outlined in the Project Management Plan. This includes project strategy, goals, timelines, functional plans (data management, clinical monitoring, and more), processes and procedures, communication pathways, and risk and contingency plans, alongside quality controls.