We are a premier drug
development research organization
About Us
We are a premier drug development research organization dedicated to advancing human health through innovative medical research. Recognizing the complexities inherent in drug development, we offer tailored solutions and strategies to accelerate the drug development process. We are committed to supporting our clients through Pharmalink’s robust Clinical Trial Management, ensuring patient safety and generating high-quality data and reports.
Solutions
Full-Service CRO
Biometrics
Clinical Monitoring
eTMF & Document Management
Medical Services
Medical Writing
Quality & Validation
Therapeutic Expertise
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.
Clinical Data Management
Accurate and Efficient Data Handling
At Pharmalink, we understand that accurate data management is the cornerstone of successful clinical trials. Our Clinical Data Management team ensures the integrity, quality, and reliability of your clinical trial data. We employ industry-leading technologies and processes to streamline data collection, validation, and analysis, ensuring your study data is accurate, consistent, and compliant with regulatory standards.
Pharmacovigilance
Ensuring Patient Safety and Regulatory Compliance
Pharmalink’s Pharmacovigilance services are designed to ensure patient safety and compliance with global regulatory requirements throughout the lifecycle of your drug. Our team of experts provides comprehensive safety management services, including the detection, assessment, and prevention of adverse effects or any other drug-related problems.
IP Management (Investigational Product Management)
Streamlined Management of Investigational Products
Pharmalink’s IP Management services provide end-to-end solutions for the management of investigational products in clinical trials. From the initial planning and manufacturing stages to distribution and accountability, our team ensures that your investigational products are managed efficiently and in compliance with all regulatory requirements.
Our team of industry-leading experts can support a variety of projects, including:
Project-specific quality planning
Fully outsourced quality infrastructure engagements
Project support through individuals and specialized teams, as needed
Therapeutic Expertise
Pharmalink provides support for drug development across all major therapeutic areas, including oncology, rare diseases, and dermatology. Our experienced team of experts supports all stages of clinical research, from early planning through trial completion to submission. With continuous education and industry involvement, our cross-functional project teams navigate complex global requirements, providing oversight to reduce risk and maximize outcomes, increasing the likelihood of trial success.
We focus on all major therapeutic areas, including drugs, biologics, diagnostics, and devices:
Anti-infectives
Auto-immune
Cardiology
CNS
Dermatology
Gastroenterology
Genitourinary
Hematology
Inflammatory
Metabolic Disorders/Endocrinology
Musculoskeletal
Oncology
Ophthalmology
Functional Service Provider Solution
Increased Efficiencies
The competitive landscape and the growing demand to swiftly bring treatments to market leave little margin for error in clinical resourcing and outsourcing decisions. Pharmalink's Functional Service Provider offering provides a skilled and tailored solution to meet the needs of your clinical development programs. This allows you to focus on your core business priorities while relying on a dependable partner to adapt to your strategic goals, culture, and needs, rapidly delivering value as an extension of your team.
Experience is Critical to the Success of Your Company
With people at the heart of everything we do and over 25 years of FSP experience, supported by our award-winning parent company, Advanced Group, which has decades of expertise in talent acquisition, strategic resourcing, and outsourcing solutions, we offer FSP solutions that stand out from our competitors.
Functional Area Expertise
Clinical Monitoring
Data Management
Clinical Trial Management
SAS Programming
Clinical (Sponsor) Oversight
Biostatistics
Pharmacovigilance and Safety
eTMF and Document Management
Site Feasibility, Identification, and Selection
Medical Writing
Site Payments
Quality Infrastructure and Auditing Services, Inspection Readiness
Investigator Grants and Contracts
Validation: CSV, GMP, GCP, GLP
Strategic Resourcing Solution
Linking Top-Notch Talent with World-Class Clinical Teams
At Pharmalink, we believe people are the heart of every clinical trial. We understand that strategic resourcing involves more than just deploying headcount, which is why we prioritize our client and candidate relationships. Our goal is to match top-tier talent with world-class clinical teams, ensuring the success of your clinical trials.
Careers
Explore opportunities to join our team and contribute to advancing global health through innovative drug development.
Contact Us
Get in touch with us for more information about our services and how we can support your clinical trial needs.