We started our corporate success with an offer on-demand consulting & recruitment services to the global Information technology industry. Soon, we earned rare recognition as the industry’s best technology and HR consultants. Since day one, our objective is to generate phenomenal value for our valuable clients by reducing costs and improving overall project productivity & quality. We have also established our vibrant presence, with an offer of full-scale, value-driven, integrated biopharmaceutical solutions. We come together with our customers to bring out new therapies to market & help, in rapidly coupling clinical performance to commercial success.
We help our customers to meet critical development milestones & optimize engagement of medical and patient communities after product confirmation.
Our clinical data managers provide you with the optimal solution for your clinical trial that will allow your study to go from first patient in to database lock as quickly and efficiently as possible without compromising data quality or integrity. We are a one-stop-shop for all data management activities from database build, through data cleaning and query resolution, to database lock and archival. Our team members are focused on developing partnerships routed in quality, efficiency, and transparency. The end result: cost-efficient data management; faster time to database go-live; a functioning, intuitive clinical database; expedited database lock; and ultimately, accurate and clean clinical trial data.
Our squad brings decades of experience to overcome the most difficult industry challenges across all major therapeutic āreas. We establish new & innovative models in scientific research with a lasting impact on the future of health care.
All our biopharmaceutical solutions comply to and uphold CDISC rules and standards to create clarity in clinical research. This means bringing together a global community of experts to develop & advance data standards of the best quality.
Our support in SDTM programming helps users to organize, normalize and manage clinical research data & metadata in compliance with company-specific in-house standards.
K2SA offers end to end data standardization services. We do ensure that your study on data and supporting documentation are compliant with Food and Drug Administration’s requirements and ready to support the regulatory review process.
By leveraging on openClinical Data Interchange Standards ConsortiumEnterprise we create FDA compliant Define.xml files. This enables easier transferral of metadata for CDISC SDTM, SEND and ADaM datasets & allows for faster time to market.
