Site Selection and Feasibility
Our expert team skillfully selects the best clinical sites for pharmaceutical companies and lab clinics. They also make sure that the sites are ideal for your clinic by performing several in-depth feasibility assessments.
Regulatory Support
By helping you complete both the local and international regulations tasks, we streamline the complex regulatory process. We also make sure that you are correctly following each and every law and regulation during the trials.
Study Start-Up Services
Our study start-up services are designed to make the clinical trials of pharmaceutical, medical and biotech companies faster. From negotiating budgets and contracts to ethics committee submissions, and providing efficient training to investigators, we handle everything.
Data Management and Biostatistics
We work with professional biostatisticians and make use of high-tech and efficient data management tools to provide error-free and specific data, high quality and accurate analysis and reporting.
Project Management
We have efficient project managers in our team who handle the entire clinical trial operation with expertise, from project planning to executing, monitoring and final finishing. They keep communicating and cooperating with all the stakeholders to keep them united.
Quality Assurance and Compliance
Quality assurance is the main focus of our services. We try our level best to follow strict quality assurance protocols so that all clinical trials can meet exceptional quality standards.
Manuscript and Protocol Writing
Our professional academic writers and subject matter experts provide high-quality and captivating manuscript and protocol writing services. They are expert in academic writing, scientific research writing and many more related to clinical research.
Ethics Committee Registrations
With our comprehensive knowledge in the field of ethics committee registration, we can help people with any issue during the ethics committee registration and guide them to successfully complete the registration by following all the steps accurately.
Trainings
Our professional trainers provide efficient GCP and GLP training that the people of the pharmaceutical and research industries require to become experts in these fields. They train people as per the GCP and GLP guidelines.
Clinical Trials
Our reliable site management services help in smooth and faster clinical trials. Our fully trained CRC staff communicates with sponsors and investigators from different locations in India to ensure streamlined and successful clinical trials in several industries.
Patent Related Services
Patentability Search
Invalidation Search
Infringement Search
Freedom to Operate (FTO)
State-of-the-Art-Search
