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"At SRC, we bring together a unique combination of regulatory, scientific and clinical expertise with business finesse to help our clients succeed in their clinical development programs to take their products to market in an efficient and cost-effective manner." –Dr. Nagendra N, Head, Clinical & Regulatory

Semler Research Center (SRC) offers clinical development services which comprehensively include a mix of innovative clinical research solutions addressing clinical development plans, protocol designs, regulatory consultation and strategy, project management & monitoring services, data management, biostatistics, medical writing, clinical supply management and archival services to address the current and emerging needs of the pharmaceutical, bio-pharmaceutical, device and diagnostic industry.

Based on a broad therapeutic experience and keen insight into the local and global regulatory requirements, SRC conducts clinical studies locally, regionally and globally, supported by expert teams from a broad network of alliance partnerships in key geographies around the world.

As an integrated clinical development service provider, we focus on providing innovative approaches to planning and conducting clinical studies across all phases of development within a framework of competitive budgets and efficient execution methodology. From clinical concept to clinical study report, the SRC team has the ability to handle large-scale clinical projects from site selection, initiation, patient recruitment, supply management and monitoring, to data capture, management, analysis and reporting — while providing due personal attention towards strategy, planning, conduct, oversight and communication.

Key Differentiators:

• Innovation & science driven approach to clinical development
• Rapid operational scalability for simultaneous IND registration across geographies
• Broad network with regional CROs across Asia(www.asiacroalliance.com), N. America & S. Africa(http://www.logictrials.com) for regional & global delivery
• Extensive regulatory expertise to navigate guidelines and streamline submissions
• Fully integrated with pharmaceutical development & manufacturing support for an end-to-end solution