Our Services

• Intuitive GUI Design/Development and Visual Presentations
• Statistical Data Analysis/Reports and Simulation Software
• Instrument, LIS and Database Interfaces
• Custom Database Development and Management
• Web-services/Web-enabled Applications
• Multi-tiered Architecture Design
• Open Standard Strategies
• Systems Integration
• Instrument/Robotics Control and Data Acquisition Software
• Experience Developing in FDA and ISO Regulated Environment
• CRSV, Software Validation, Systems IQ/OQ/PQ
• Disaster Recovery Planning for Critical Systems

Our Process

• Consultative Approach -
  At The Ashvins Group, we place an emphasis on learning our client's business.
  
  
• Personal Attention -
  Each client is assigned a project manager who guides decision-makers through the development lifecycle.
  
  
• Formalized Development Process -
  Our Software Development Lifecycle is specifically tailored to rapid-development and is based on the Rational Unified Process.
  
  
• Manageable Steps -
  We breakout schedules based on key milestones and delivery of project artifacts.
  

• The Ashvins Group works with industry-proven software tools, databases and application server systems from Borland, ORACLE, Microsoft, Sun and IBM.
  
  
• Our Accelerators are fluent in wide variety of programming languages, tools & standards, including Java, J2EE, Perl, Python, C/C++, .NET, Delphi, Kylix, JBuilder, VB; apply XML, SOAP, JDBC, ODBC and TCP/IP standards.
  
  
• We go beyond the role of technology provider to become a technology partner. We focus on knowledge transfer from conception and design to implementation and operation.

• Rational Unified Process guides development and implementation activities.
  - "Use Case" analysis to facilitate Requirements Engineering
  - Iterative development cycles to minimize risk and optimize development time
  
  
• Development of key artifacts throughout the cycles.
  
  
• Project review and milestone monitoring via Sponsor Team approach.
  
  
• Rigorous Risk Management and Change Management Process.
  
  

• IT skills PLUS laboratory oriented knowledge to facilitate communications and understanding of end-user requirements.
  
  
• Training in Clinical and Life Science applications, instrumentation and data models.
  
  
• Experienced in FDA and ISO regulations.

Our Product

Computer Related System Validation (CRSV)
Powerful software designed to make validation easier

ValidationBUILDER™ software helps minimize resources and time required for CRSV. This intuitive software assists Project Leaders in the pharmaceutical, biotech and clinical fields in validating Computer Related Systems used to automate laboratory procedures, consolidate data collection and analysis, and run sophisticated QC or manufacturing operations. No matter how simple or complex the validation project, ValidationBUILDER leads the user through the process, provides standardized documentation templates that are based on FDA guidelines, and generates final reports. ValidationBUILDER supports validation of off-the-shelf software (OTS), configurable systems and application specific software.