CLINICAL TRIALS
Conduct of Clinical Trial (Phase I to Phase IV, BA/BE, Biomedical Heath Research).
250+
Research
ABOUT US!
Prerna Clinical Research (PCR) is a unique Site Management Organization (SMO), initiated to fulfill growing demand for clinical research trials in India. In order to keep pace with global requirement there is a need for SMO to provides support to the hospitals, medical colleges, pharmaceutical, biotechnology and medical device industries in the form of research services outsourced on a contract basis and to coordinate the conduct of clinical trials with global & local guidelines and regulatory requirements..
Prerna Clinical Research (PCR) started with vision to accelerate the clinical research growth in India. PCR is continuously engaged in providing various services and expert professionals for Clinical Research & Training industries.
Mission
Conducting clinical trials on Ethical way to ensure best product development.
vision
Assisting discoveries to the best possible level and contribute to the new and advance medication.
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Planning
Planning and execution of clinical trials.
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Conducting
Conducting ethical clinical trials on site and achieving recruitment target.
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Information
Information and partnering solutions with highest quality.
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Attention to details
Attention to details and focussed on the needs of the client.
- Strong capability in study design and execution as required by local laws, GCP standards & client SOP’s.
- Dedicated team for each project with a one point contact for client.
- Highly experienced team with specialization in this field.
Advantages of PCR
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Zero deviation: -
- We are not only committed to meeting the targets of our clients, but also monitor the individual project steps to ensure maximum transparency and credibility.
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Attention to detail: -
- We consider active listening, precise research, solution finding and consequent action as the foundation of our services.
- Our key principles are correctness and accuracy of the data and maintaining the integrity of the said data.
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Employee strength: -
- Our employees are our biggest asset; we provide continuous training and constantly focus on their skill development to provide the highest customer experience.
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Quality assurance: -
- Inspection of critical phases of study, procedures, site and subcontractor facility (equipment, computer system, archives).
Project Management:
- Project planning, documentation and tracking
- Budget management and resource management
- Risk analysis and contingency planning
- Management of project timelines
- Constant team and client communication and reporting
- Project-specific team training
- Development of project-specific procedures and guidelines
- Quality management together with Head of Quality Assurance
- Strong managerial skills
Explore Our Services :
Site (Hospital) management for clinical studies
Develop and manage hospital for conduct of clinical trials.
Ethics committee
Assisting hospital for registration of Ethics Committee.
Clinical Research Training
Provide training on guidelines and regulation related to clinical research to clinical research aspirant and professionals.
Monitoring
Outsource of third-party monitoring.
Team Of Prerna Clinical Research?
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Physicians, Management Executives, Pharmacy Graduate/Post Graduate; Alternate Medicine Graduates are our core team members. Team at Prerna Clinical Research (PCR) has rich experience in the area of Clinical Research, Medicine, Management, Technology and Finance.
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Prerna Clinical Research (PCR) team has strong hand in conducting & managing clinical trials in different therapeutic area at multiple locations.
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Prerna Clinical Research (PCR) team has strong hand in conducting & managing clinical trials in different therapeutic area at multiple locations.
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Our Clinical Research Coordinators (CRCs) are trained on clinical research guidelines, regulatory requirements and experienced in conducting clinical trials. We take great care to ensure that they have all the skills and capabilities required to deliver expected results. We have the best site management personnel dedicated to bring out the best in our highly trained and experienced clinical trial teams.
Clinical Operation
- Standardized selection procedures of Clinical Sites
- Consistent, high quality and cost efficient model
- Performance of all contractors evaluated on regular basis and reviewed by QA auditing process
- Achieving recruitment target within timeline and generating authentic and quality data
Therapeutic experience :
- Anti-infective
- Cardiology
- Dermatology
- ENT
- Endocrinology
- Gastroenterology
- Gynecology
- Hematology
- Immunology
- Neurology
- Nephrology
- Obesity
- Oncology
- Ophthalmology
- Orthopedic
- Osteoarthritis
- Psychology
- Respiratory
- Rheumatology
- Sexology
- Urology
- Women’s healthcare
Career Of SMO
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In PCR we believe our employees are our asset and career. We give platform for those who want to grow at apex stage in their career.
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We provide them favorable atmosphere and serve as the ladder by giving all opportunities to showcase their talent.
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We at PCR work in making mutual wealth with our employees.
