Our Services
The feasibility process is the fundamental of our project management. TCRS has worked on every therapeutic area and has an association with key investigators and trial sites. We select the best investigative sites to manage a clinical trial with the help of our efficient feasibility assessment process. We have well-experienced feasibility and site selection team to visit the sites and examine the site facilities for managing clinical trials.
TCRS has experts on handling budget in their team. The team helps sites or work as a connector between sponsor and site.
Our team makes sure to maintain accuracy and quality throughout the conduct of clinical study. TCRS has maintained the process of excellent quality management and monitoring throughout the trial. Also, the QA person helps CRC to prepare the site for Sponsor monitoring or audit.
Our expert’s staff prepares the regulatory documentation as per the requirement of Ethics committee submission. We follow the EC SOP and guidelines and manages to get approval from EC in timeline.
TCRS has highly trained and experienced staff for project management from start up to close out.
Our aim is to ensure quality in project management along with a timeline of associates.
TCRS makes sure that we have successfully managed a clinical trial with quality, ethics & guidelines and our approach toward clients helps them to address risk assessment and mitigation plan in detail.
We have Standard Operating Procedures (SOPs) which are uniformly written procedures, with detailed instructions to record routine operations, processes and practices which will be followed within our organization.
In clinical research, SOPs help defines the standard practices and daily processes conducted to assure execution of research tasks in accordance with institutional, state and federal guidelines.
Our SOPs contain adequate detail to clearly guide research staff through a particular procedure and thereby establish uniformity in the everyday functions of the department.
Our SOP have a specific aim but we have written in a general format that can be easily followed.
By laying out defined processes, the primary function of our SOP is to specifically avert procedural deviations.
TCRS prepare documents as per the guidelines of CDSCO & helps our associates/IRB’s to apply for registration & re-registration.
reach out us
If you are interested in learning more about how TCRS can support your clinical trial management needs, please feel free to reach out to us . We would be happy to schedule a call or meeting at your convenience to discuss further.
Thank you for considering Trialcraft Clinical Research Services. We look forward to the possibility of working together to advance the field of clinical research.