SAS

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SLP is managed by a team of professionals who have over the years gained adequate experience in providing solutions to all manpower recruitment needs. We are currently a team of 15 consultants, specializing in different domains across industries, who professionally “head hunt” candidates around the country through various contacts and networks.

By leveraging our experience and skills to design and implement successful products and strategies, we enable our clients to achieve their operating and financial goals from niche providers to multi-national enterprises.

We are in the business of effectively understanding your manpower requirements, procuring the candidate with the desired profile and building trusting relationships. With our industry expertise, we understand that company’s today require more than a skilled candidate; they reach for employees who are productive, exhibit a positive attitude and have the ability to become a member of their team.

Clinical Data Management

At SLP, our clinical data management and consultancy services are dedicated to providing you with clinical data, data analysis, regulatory support and presentation requirements.

The increasing role of a dedicated Clinical Research Organization in your company's clinical data requirements.

At SOFT SOURCE, our clinical data management and consultancy services are dedicated to providing you your clinical data, data analysis, regulatory support and presentation requirements. Within clinical data management, optimal therapeutic designs, customer support and customized data analysis are key areas where our bio statisticians and medical writers interact to provide comprehensive solutions. Only through an all-inclusive understanding of study objectives, clinical design issues, and upgraded quality control measures, can maintenance of the quality of data and adherence to expected deadlines be achieved. Analysis of clinical trials includes pharmacokinetic and dynamic evaluations, therapeutic equivalence testing and sequential designs.

Our Clinical Data Management Services
  • CRF Development
  • Case report form design, production, and tracking
  • Clinical Data Entry
  • Data entry cleaning
  • Case report form review
  • Automatic edit checking and query tracking
  • Medical Coding
  • Coding of adverse events (meddra, who-art, costart)
  • Coding of concomitant drugs (who drug centralized data coding)
  • Clinical Database locking
  • Crf-Annotation
  • Clinical Data transfer specification (CDISC-SDTM and Sponser specific)