What we offer
People Value
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Client Value
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Societal Value
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At CCRSPL, we believe that excellence is not a one-time act, but a continuous habit—refined through consistent training, ethical practices, and a strong work culture. Our commitment to quality is deeply rooted in our daily actions, making excellence not just a goal, but a way of life.
We proudly operate as both:
A leading Site Management Organization (SMO) in India, providing end-to-end solutions for clinical trial execution.
A premier Clinical Research Training Institute, offering industry-relevant education to aspiring life science professionals across the country.
Staying aligned with the latest trends and regulatory updates in clinical research, we continuously enhance our services to meet evolving industry demands. At CCRSPL, our goal is to deliver value to sponsors, support principal investigators, and empower the next generation of clinical research professionals.
Our Services to Sponsors & CRO
Feasibility & Site Selection
Subsequently, the feasibility process is the fundamental of our project management. CCRSPL has worked on effectively every therapeutic area and has an association with key investigators and trial sites. Our services include the selection of the best investigative sites to manage a clinical trial with the help of our efficient feasibility assessment process. Also, we have well-experienced feasibility and site selection team to visit the sites and examine the site facilities for managing clinical trials.
Project management : Start up to close out
CCRSPL has highly trained and experienced staff for project management. Our goal is to ensuring quality in project management along with a timeline of associates. Additionally, our team makes sure that they have successfully managed a clinical trial with quality, ethics & guidelines. With their proactive approach toward clients helps them to address in detailed risk assessment and mitigation plan.
Handling Budget for Site
In Addition, budget is a very crucial task in project management. Here, CCRSPL has experts on handling budget in their team. The team helps sites or work as a connector between sponsor and site.
Quality Assurance/ Monitoring
CCRSPL team makes sure to maintain accuracy and quality throughout the conduct of clinical study. CCRSPL has maintained the process of QA by its Project manager throughout the trial. Also, the project manager helps CRC to prepare the site for Sponsor monitoring or audit.
EC Submissions
On the top of that, CCRSPL expert’s staff prepares regulatory documentation as per requirement Ethics committee submission. So, we follow the EC SOP and guidelines. Manages the hurdles to get approval from EC in timeline.
Our Services to Investigator or Sites
Providing expert staff on Clinical Research
Clinical researchers can add on some expertise resource for complex trials, not only for more guidance but also for the assistance partnership with investigators. So that to get knowledge of study design, initiation, manage and results. CCRSPL provides theses facility to the researchers.
SOP Writing
Standard Operating Procedures (SOPs) are uniformly written procedures, with detailed instructions to record routine operations, processes and practices followed within a business organization. In clinical research, SOPs help defines the group’s (e.g., unit, division, department, institution, etc.) standard practices and daily processes conducted to assure execution of research tasks in accordance with institutional, state and federal guidelines.
SOPs should contain adequate detail to clearly guide research staff through a particular procedure and thereby establish uniformity in the everyday functions of the department. Each SOP should have a specific aim but be written in a general format that can be easily followed by a broad audience. By laying out defined processes, the primary function of an SOP is to specifically avert procedural deviations.
Project management team support to investigator
CCRSPL’s project management team have some responsibilities. Their primary goal is to accomplish the tasks allocated to them by the project manager. The progress of the task should be discussed with the lead by the members, and if there is any problem or changes the team expected to inform it immediately to the Manager.
Our team knows the importance of their roles and responsibilities which helps to make the project successful.
Archival Support as per the Guidelines
Most importantly, CCRSPL act as third party vendor for archival of clinical study documents as per the requirement of our associates & guidelines.
Our Services to the Ethics Committee
CCRSPL prepare documents as per the guidelines of CDSCO & helps our associates/IRB’s to apply for registration & re-registration and also for NABH accreditation.
Canvass Clinical Research Services Ltd has received recognition from government of India for being the start up company in the Healthcare Industry. The recognition is from the Department for Promotion of Industry and Internal Trade(DPIIT). Moreover, we have received the UDYAM certificate from the Ministry of Micro, Small and Medium Enterprise. Also, we have the ISO 9001: 2015 accreditation.
Being the best site management organization in India, we have experts who work for the clinical trials effectively. Till now , our clinical trials has been taken place in Maharashtra, Madhya Pradesh and Chhattisgarh. That's why, we ranked in the site management organization list in India. Above all, our studies and researches till now are to the point and helpful to the principle investigators as well as to the patients.
Additionally, we work as an institute to provide quality knowledge of clinical research to the students from pan India.