About Us
About Us
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 Technologies 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 Technologies 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.
Vision
To change lives for the better
Mission
To improve and accelerate the delivery of therapies, thereby reinforce each patient’s hope for a healthy and happy life.
Why SCL?
- Accelerate customer performance
- Help guide decision making and investment
- Evolve future-focused, and actionable insights
- Partner in insights-driven product development
- Offer robust and quality based cross functional solutions
- Provide for greater therapeutic coverage (21 medical specialties)
- Drive change with equal focus on health lives, clinical impact and commercial success
- Wider global reach with focus on North America, Europe, Middle East and South Asia
- Bring together seasoned clinical and business minds to address modern market realities
- Collaborate with the global bio-pharmaceutical industry to better execute and succeed in a constantly evolving environment
Team
SCL IT Technologies is driven by a set of principles and established ethics. Our customers’ immediate and emergent needs are our primary concern. As a team of trusted and experienced personnel, we are concerned with offering end-to-end support to the biopharmaceutical businesses on research, data analysis and compliance with global standards. Surely, patients are waiting for a therapy that could change their lives. So, our teams’ combined efforts are channeled towards promoting biopharmaceutical research, enhancing capacities and capabilities, providing compliance to global standards, and working in the best interests of patients.
Our team of experts helps to leverage on end-to-end capabilities and global functional, therapeutic and highly customized solutions. Beyond developing high-value strategic plans our team also delivers useable, practical solutions and collaborating with your team in portfolio and product strategy, organizational design and implementation. Our team members work as transformation agents who can address some of the industry’s most pressing problems.
Our team brings a strong technical understanding of both Study Data Tabulation Model (SDTM) analysis Data Model (ADaM), relating to implementation and Reviewer’s guides, CDISC terminologies and the related regulations. The team of trained and experienced resources enables us to deliver high-quality datasets at a cost saving of 20% to 40% compared with traditional service providers.
The strengths of our team include,
- Help the global biopharmaceutical industry to view lifecycle management beyond the clinical space
- Define areas for growth through our scientific expertise and business acumen
- Further studies and analyses in the economic impact of treatments, diseases and conditions, including the direct costs of medical expenditures and indirect costs
- Provide everything from a go-to-market strategy, including brand planning, launch planning, launch readiness, launch management, competitive simulation and performance tracking
- Help to gather market information or conduct cost analyses both enabled by our robust analytics
- Help to generate captivating content that best communicates our customers’ strategy-driven messages
- Evolve a combination of proven analysis methodologies, commercial models and therapeutic expertise, combined with the power of our broad set of commercial and clinical capabilities
