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Avigo is led by an experienced management team with a history of success in developing comprehensive solutions within the Life Sciences and Information Technology sectors. 


With facilities and staff both in the US and offshore, Avigo’s team members collaborate with clients to develop comprehensive solutions that meet a Life Sciences organization’s present and future data requirements. The team’s deep domain knowledge consistently allows it to rapidly deliver results-oriented R&D solutions. 

Our clients include prominent pharmaceutical, biotech, medical device and lab diagnostics companies.


Our client projects have spanned the R&D life cycle, from pre-clinical through commercialization, and include requirements definition through technology development.

 

Avigo Solutions is a leading provider of consulting services to Life Sciences, Healthcare and Technology industries.  


The company focuses on optimizing clinical and regulatory functions, including clinical trial protocol design and data management, patient recruitment and engagement technology, clinical registries and regulatory affairs information management.


Our team has delivered several key projects for clients. A subset of recent engagements include:

  • the development of requirements, architecture and prototypes for a comprehensive patient recruitment, retention and engagement platform using patient lab, genomic, prescription and medical history data for a major lab diagnostics client. 
  • the development of patient communities and registries for disease-specific foundations/groups,
  • the provision of clinical trial data management services, including CDISC transformations and statistical analyses for pivotal trials at a transnational biotechnology company
  • the development and maintenance of a regulatory information management solution, including xEVMPD/IDMP aspects for a generic drug manufacturer
  • pharmaceutical R&D system management and cGxP compliance services for an oncology-focused biotech company.

Avigo’s core offerings are based on the practical implementation of integrated solutions that enhance decision-making capabilities in R&D. At a broad level, our offerings encompass requirements definition, product strategy, system architecture and design, development and integration, and operations support solutions. Specific areas of expertise include the following:

  • Patient recruitment and engagement technologies
  • Clinical registries, including QI registries, and Patient communities
  • Clinical trial protocol optimization and clinical trial data management, including CDISC transformations
  • Regulatory information management, including management of HA interactions , CMC change assessments, contacts/commitments, submissions and registrations
  • IDMP data rationalization 
  • Drug Safety and Labeling solutions
  • Regulated document management
  • Pharmaceutical R&D systems management
  • 21 CFR Part 11, HIPAA and cGxP compliance