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SIRO is a full- service clinical research organization with experience in all phases of clinical trials and in all key areas of the drug development process.
You can count on SIRO to support all aspects of your clinical development plans in India.
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Clinical Trials
From an Idea to an approved product, a drug's journey through the complex development process is often anxiety -filled. The most critical component in this process is clinical development. It is very critical for a company to make sure that the identified opportunity has the best chances for success. Clinical trials account for the largest component of the cost and the timelines, and also the greatest risk for things to go wrong. Each phase has its own set of challenges and you need a partner that has seen it all and is capable of meeting your needs from phase I to IV.
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At SIRO, it is our endeavor to make sure that all studies receive a high level of attention to detail, the same quality of clinical services and regulatory compliance. To ensure this we offer you our experienced project managers and multifunctional study teams.
The teams work closely with investigators, patients, and sites and are backed by tools and processes that are designed to avoid the many pitfalls that often plague clinical trials. Our teams are trained to ensure that all protocols are followed and deadlines met.
Our proactive and creative approach to ensure the acceleration of the clinical trial is what keeps our clients satisfied with our services and ensures a high level of repeat business.
We invite you to explore our services that can be sourced invidually or as a part of a full scope study.
Feasibility and patient access planning
Project Management and Planning
Clinical Monitoring
Medical Services
Clinical Audit Services and Quality Assurance
Other related services that can be sourced individually
Site contract management
Clinical resourcing
Investigator recruitment
CRF design
Clinical data management
Biostatistics
Medical Writing
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