We Are Here With Best Services

At CCRSPL, our services reflects the fact that excellence is won by training & habituation. We do not act rightly because we have virtue or excellence, but we rather have those because we have acted rightly. Canvass is what we repeatedly do. Excellence, then ,is not an act but a work culture. Moreover, we work as a leading site management organization in India and as the best institute of clinical research courses in India. Furthermore, CCRSPL believes to enhance our services on continuous basis by remaining updated with the latest clinical research trend.

We Are Here With Best Services

At CCRSPL, Excellence is won by training& habituation. Above all, we do not act rightly because we have virtue or excellence, but we rather have those because we have acted rightly. We are what we repeatedly do. Excellence, then ,is not an act but a work culture.

Our Services to Sponsors & CRO

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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.

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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.

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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.

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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.

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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 Sponsors & CRO

Z

Feasibility & site Selection

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. 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.

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Handling Budget for Site

Budget is a very crucial task in project management.  CCRSPL has experts on handling budget in their team. The team helps sites or work as a connector between sponsor and site.

Z

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. 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.  

Z

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.

Z

EC Submissions

CCRSPL expert’s staff prepared regulatory documentation as per requirement Ethics committee submission. We follow the EC SOP and guidelines. Manages the hurdles to get approval from EC in timeline

Investigator or Sites

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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.

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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.

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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.

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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.

Ethics Committee

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. 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.

 

CCRS india

Our projects are beneficial for the patients as well as for the sponsors because we ensure the study protocols to run on budget and on time. In any trial, Feasibility assessment plays a significant role and identifying the feasible site and investigators is our responsibility.

With our experienced project managers as well as clinical research coordinators, we believe in  providing the best site management services. In addition, our team not only looks after the research part but also the documentation part very effectively.