| SMO Clinical Research (I) Pvt Ltd (SMO-India) was established and privately held since 2007, is a Contract Research Organization (CRO), head quartered in the heart of India's healthcare services and IT hub, Bangalore. SMO Clinical Research (I) Pvt. Ltd is a registered CRO under the Central Drug Standard Control Organization (CDSCO) and operates in full compliance with the New Drugs and Clinical Trials (NDCT) Rules, 2019. SMO-India has been providing exceptional Site Management and Project Management, and Monitoring of Phase I, II, III, and IV clinical trials involving Pharmaceutical, Biological, and Medical Device products to its clients. We maintain 100% retention of our clients due to our commitment, responsiveness, flexibility, performance, cost-effectiveness, and unmatched quality. We complement each client's working culture and management style and are flexible to their requirements. |
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| SMO-India delivers cost-effective, quick-to-market clinical services in emerging and traditional markets of research, along with experience in a broad range of therapeutic areas and phases of development. The critical success factor for SMO-India has been the robustness of its operating procedures and a deep understanding of the guidelines and regulations governing clinical research. We have sharp business insight to address the right opportunity in the right manner, and the team is appropriately trained to execute the projects efficiently and deliver high-quality work on time. Our sole objective is to support the desired outcome of clinical trials through expeditious enrollment of appropriate patient populations in a sustained and globally acceptable manner. Our experts work with sponsors to minimize risks and establish contingency plans, providing strong quality and regulatory controls to ensure protocol compliance and patient safety. |
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| Our Vision | ||
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| Our vision is to charter new frontiers of medical and pharmaceutical science and technology by excelling in providing true-blue professional services in the realm of Clinical research. | ||
| Our Mission | ||
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| Our mission is to establish ourselves as India's trail-blazer Contract Research Organization by weaving a network of highly qualified and experienced clinical researchers and healthcare professionals with demonstrated expertise in conducting clinical trials and to maintain the highest standards of quality, time-sensitivity, unwavering commitment to excellence, and uncompromising compliance with the statutory regulations in initiating, conducting, controlling and comprehensively managing the Clinical operations. | ||
| Core Values | ||
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| Our Expertise | ||
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| SMO India has exceptionally qualified staff with clinical trial experience in managing Phase trials in a broad spectrum of therapeutic areas. We have the scientific and clinical expertise to take a trial from concept to completion, as well as combining all of the functional areas of a CRO to conduct Phase I, Phase II, Phase III and Phase IV clinical trials. Our experience gained through global exposure to clinical studies allows us to understand clinical study requisites and objectives. This knowledge and experience enable us to guide clients to formalize an optimal development plan and strategy that will shorten trial time and produce uncompromised data and results. We have access to highly skilled sites and provide site specific guidance and support. The highly motivated team supports upbeat Ethics Committee management, patient recruitment and patient retention. Thus, enabling the investigators to dedicate time to focus on the patients, and ensure that the study is conducted in the highest standards of quality, ethics and performance. This support ensures collection of high quality study data necessary for regulatory and product approval submissions. SMO India is an assurance for in-depth pre-study planning, most appropriate and nearly accurate feasibility data, most favorable patient recruitment rate, transparency in communication between sites and all parties involved.
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| Our Expertise | ||
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| SMO India has exceptionally qualified staff with clinical trial experience in managing Phase trials in a broad spectrum of therapeutic areas. We have the scientific and clinical expertise to take a trial from concept to completion, as well as combine all of the functional areas of a CRO to conduct Phase I, Phase II, Phase III, and Phase IV clinical trials. Our experience gained through global exposure to clinical studies allows us to understand clinical study requisites and objectives. This knowledge and experience enable us to guide clients to formalize an optimal development plan and strategy that will shorten trial time and produce uncompromised data and results. We have access to highly skilled sites and provide site-specific guidance and support. The highly motivated team supports upbeat Ethics Committee management, Patient Recruitment, and Patient Retention. Thus, enabling the investigators to dedicate time to focus on the patients and ensure that the study is conducted in the highest standards of quality, ethics, and performance. This support ensures the collection of high-quality study data necessary for regulatory and product approval submissions. SMO India is an assurance for in-depth pre-study planning, the most appropriate and nearly accurate feasibility data, the most favorable patient recruitment rate, and transparency in communication between sites and all parties involved. |
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