About Us

SCL IT is headquartered in Hyderabad, India. We started our corporate success with an offer of on-demand consulting and recruitment services to the global IT industry. Soon, we earned the rare recognition as industry’s best technology and HR consultants. Since day one, our objective is to generate phenomenal value for our clients by reducing costs and improving overall project productivity and quality. We have also established our vibrant presence, with an offer of value-driven, full-scale, and integrated biopharmaceutical solutions. We collaborate with our clients to bring out new therapies to market, and help in rapidly bridging clinical performance to commercial success.

SCL IT delivers value to small, medium and large bio-pharma industry by leveraging on its unique bio-pharma model which is repeatable, predictable, and highly reliable. We help our clients to meet critical development milestones and optimize engagement of medical and patient communities after product approval. We offer focused, competitive and FDA compliant support services to the global biopharmaceutical industry. Our focus is on biostatistics, CRO, Statistical Programming, SAS programming, CDISC Services, SDTM and ADaM Programming, Pinnacle 21, Define XML, etc.

SCL IT pioneers full-service contract research organization (CRO) services. Our CRO services are built on high level of collaboration and flexibility. We take care of the local regulatory requirements through our proven CRO expertise and therapeutic leadership. Our team brings decades of experience to overcome the most difficult industry challenges across all major therapeutic areas. We establish the new and innovative models in clinical research with a lasting impact on the future of health care.

All our biopharmaceutical solutions adhere to, and uphold CDISC norms and standards to create clarity in clinical research. This also means to bring together a global community of experts to develop and advance data standards of the highest quality. Our support on SDTM programming helps users to organize, standardize and manage clinical research data and metadata in compliance with CDISC SDTM or company specific internal standards.

SCL IT offers end to end data standardization services. We ensure that your study data and supporting documentation are compliant with FDA's requirements and ready to support the regulatory review process. By leveraging on OpenCDISC Enterprise 2.5 we create FDA-compliant Define.xml 2.0 files. This enables easier transmission of metadata for CDISC SDTM, SEND and ADaM datasets and also allows for faster time to market.