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  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. Since then SMO-India has been providing exceptional site management and project management and monitoring of phase II, III and IV clinical trials involving pharmaceutical, biological and medical device products to its clients. We maintain High 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.  
  SMO-India's working model has been SMO within the CRO. This working model has helped our professionals to ensure client satisfaction through streamlined procedures that provide rapid turnaround of tasks, enabling faster start up and compliance with applicable guidelines. This working methodology is most suitable for the onsite trial management in addition to monitoring and Project management services. Specializing in global patient recruitment, we start by accurately identifying target patient populations through feasibility and implementing cost-effective strategies and tactics to complete enrollment on time. Our recommendations based on feasibility analysis have saved sponsors significant clinical development costs through enhanced protocol design modifications and reduced recruitment periods. SMO-India conducts feasibility by a dedicated feasibility team. By assessing potential investigators at the site level, we have a more accurate analysis of their workload and competing studies. Investigators are recruited based on their past history of patient recruitment, data quality, and feasibility report based on the specific protocol. 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 their operating procedures, 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 who is appropriately trained to execute the projects efficiently and deliver high quality on time. Our sole objective is to support the desired outcome of clinical trials through expeditious enrollment of appropriate patient population 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.  
  Our Vision  
  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 site management.  
  Our Mission  
  Our mission is to establish ourselves as India's trail-blazer Site Management 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  
  • We ensure research subjects are fully apprised of all the risks & benefits arising in and out of the study.
  • We strictly adhere to the principles governing the privacy and confidentiality of the research subjects.
  • Care and caution are our watch words at all stages of the research to ensure that the research subject is not put to undue risk.
  • We ensure the research is conducted only by competent and qualified persons who act with total integrity and impartiality.
  • We conduct the research in a fair, honest, objective and transparent manner after full disclosures are made of each aspect of their interest in the research by all those associated with the study.
  • We strictly observe principles of compliance.
  • We provide services in a most cost-effective manner without compromising on quality.
  Our Expertise  
  SMO India has exceptionally qualified staff of about 40 with a clinical trial experience in managing Phase trials in 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 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.

Therapeutic areas: including Pediatrics.
  • Oncology
  • Endocrinology
  • Cardiovascular
  • Dermatology
  • Infectious Disease
  • Medical Device
  • Inflammation (Rheumatology)
  • Neurology
  • Gynecology
  • Gastroenterology
  Our Expertise  
  SMO-India’s exceptionally qualified staff have over 25 years of domain clinical trial experience in managing over 70 trials in a broad spectrum of therapeutic areas. We have the ability to guide our clients from initial trial planning stages to regulatory submissions phase. 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.