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| The SIRO Advantage |
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SIRO Clinpharm is a leading full service Clinical Research Organization that specializes in providing solutions to the twin challenges of speed and cost in clinical drug development. We have pioneered the development of alternative geographies for conducting clinical trials, providing world class facilities, expertise and unexplored patient pools. For over a decade now, our clients from North America, European Union and Japan have utilized our expertise to significantly accelerate clinical trials and reduce costs.
We have been rated as the best Indian CRO several times and most recently selected as the Frost and Sullivan 'Partner of Choice' for clinical trials in India. What makes us the partner of choice is a series of advantages that ensure that your decision to partner with SIRO for clinical trials in India is indeed your best bet for your clinical development plans in India. A few reasons as to why, global pharma and biotech companies increasingly chose to work with SIRO.
The most experienced Indian CRO
SIRO was established in 1996, a time when global clinical trials in India were few and far between. For more than a decade now we have pioneered the growth of the clinical trial industry in India and in the process have gained significant experience in all aspects of clinical development. We are probably the only Indian CRO that has worked in all the key therapeutic areas and across all phases of clinical development, data management and biometrics.
The most trusted Indian CRO
Over 80% of clients that have worked with us continue to consider SIRO for their clinical development needs in India. We have worked with 9 of the top 10 pharmaceutical companies and have also proved to be an equally committed partner to small and midsized companies. Our services have been audited by global clients with no major findings and we are in long term ongoing relationships with leading global pharma. The trust is reflected in the various awards we have won.
The largest, independent, full service Indian CRO
With team size of 400 and growing SIRO offers the complete range of solutions for phase I to IV clinical trials. We work with over 250 sites across more than 40 cities in India. We have one of the largest data management and biometrics set ups among CROs in India and have the necessary scale and management bandwith to deliver on large projects. SIRO is exclusively focused on clinical R&D and has never merged in to or has been acquired by any other company in the past.
Globally accepted quality
SIRO has submitted data for successful regulatory submissions to USFDA, EMEA, UKMHRA, Korean FDA, WHO, Health Canada and DCGI. We have worked with clients from North America, European Union and the Asia pacific. Over 80 % of SIRO's work experience has been in global clinical trials and our quality standards have been matched and found to be at par with the best worldwide.
High service levels
SIRO believes in working as an extended arm of its client team and a key reason for our success in working with diverse clients is our ability to go the extra mile in allocating adequate resources to projects as well as a proven system of ongoing feedback that ensures that the clients are always in control of their projects. We offer customized solutions - full-phase clinical trials, single-phase trials, consultation or other solutions based on client need. Our presence in the USA and shortly in Europe is designed to provide local support for all projects.
A track record that inspires confidence
- Managed > 150 studies (Clinical) & > 200 studies (Clinical data management and Biometrics)
- Over 15,000 clinical trial subjects recruited
- Working with > 300 hospitals and medical centers across >40 cities
- Successfully passed > 140 Audits by Sponsor QA teams
- Experienced in managing complex protocols on a wide spectrum of therapeutic indications
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