Solutions

The process of determining if a specific clinical program or trial can be conducted in a given geographic area with the ultimate goal of completing the project as efficiently as possible in terms of budget, schedule, and deadlines is known as clinical trial feasibility.
Clinical features, site demographics, recruitment and retention, ethical considerations, site infrastructure, and quality are some of the criteria that clinical trials use to evaluate data.
Measurement of adherence to delivery pledges; turnaround times for feasibility requests; startup documentation requests; and data collection during study execution.A regular quality assurance (QA) process has been carried out for the studies. Quality output measurement includes building metrics around the variability between what was promised during feasibility and what was actually delivered, data queries per patient per study, how these trends are measured, how many monitoring follow-up action items were sent to the site, and the number of resolved and unresolved queries after 15 days, 30 days, and three months.

Assists in choosing a site based on factors such as education, expertise, training, past work on related trials, the infrastructure and site team of the investigator, Anything else that is necessary for the trial and particular to the protocol

Clintrials provides ICH-GCP,New Drug and Clinical Trial rules, ICMR, Schedule Y, National Ethical guidelines for Human Participants for PI, Co-I,CRC, Phlebotomist, Study Nurse and other team members.

Examine Starting with suggestions from knowledgeable people and possible locations.
submission of study documents to the ethics committee.
Study viability and preliminary documentation preparation at the site level.
Recruitment of subjects and subsequent monitoring.
Helps in patient recruitment in large quantities and offers creative ways to broaden the patient base.

Timely updates and high-quality documentation.
quick EDC completion and query resolution.
Fast-track data submission to CRO/Sponsor accessible around-the-clock for SMO services.
Document storage facility in accordance with legal requirements.

Clintrials makes it easier to submit and get trial-specific materials approved in the manner necessary by the IRB and/or IEC. This includes keeping track of the IRB/IEC meeting calendar centrally, as well as the document/format and number of copy requirements for each IRB/IEC and cover letter requirements, among other things. As required by local regulations, we guarantee the prompt filing, tracking, and presentation of approvals and letters, along with quality control checks. The Clintrials central analytics team helps the sites during the study by notifying them of SAEs/SUSARs and providing annual status reports to the IRB/IEC or regulatory authorities as needed. Because this is centrally managed throughout the Clintrials network, it takes less work for the sponsor, CROs, and site.

Clinical Trials The infrastructure that sponsors and investigators require consists of physical infrastructure (such as project rooms and storage), ethical infrastructure (such as regular committee meetings and reviews), and resources (such as CRCs, study nurses, Phlebotomist, and co-investigators). Methods and measurements to gauge progress, include into clinical trials, demonstrate ongoing and finished projects with us, and establish procedures and measurements that will help us reach our long-term goals.

Principal Investigators.
Co-Investigators.
Clinical Research Co-ordinators.
Study Nurses.
Phlebotomist.
Other professionals.

EC Members association and ICH-GCP Training.
SOP Preparations.
SUGAM Portal (CDSCO) Registration/Re-Registration.
NAITIK Portal (DHR) Registration/ Re-Registration.
NABH Accrediation of IEC.
EC Co-ordinator services.

i.Healthcare Provider Partnerships:
Collaborate with local healthcare providers, hospitals, clinics, and physician networks to raise awareness about clinical trials among patients and referring physicians, and facilitate patient referrals.

ii.Website Optimization:
Ensure our website is user-friendly, informative, and optimized for search engines to attract potential participants who are actively searching for clinical trial opportunities online.