We pride ourselves in being able to offer our clients customized solutions to meet their demanding business needs.

Our Services

Anovo is a consulting group specializing in solutions that span the entire biopharmaceutical life-cycle adapted for large, medium, and small pharmaceutical and biotechnology organizations. Anovo offers an unparalleled experience, comprehensive capabilities to meet and exceed the most demanding business objectives while optimizing limited resources.


Anovo provides clients with a broad portfolio of innovative clinical solutions such as:

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Clinical Site Management

  • Budgeting and contracting
  • Site and investigator identification and selection
  • Subject recruitment, compliance, and retention


Project Management

  • Project Plans
  • Resource planning and allocation
  • Risk assessment and management


Clinical Trial Solutions

  • Ancillary study manuals design and development
  • Central IRB selection and submissions
  • Clinical monitoring plan design and development
  • ICF template development and review
  • Investigational brochure design and development
  • Investigational product sourcing and logistics
  • Protocol design and development
  • Safety and endpoint committee charters design and development
  • TMF development and maintenance (central and investigative site files)


Vendor Selection

  • Contract negotiation services
  • RFP process management
  • Vendor management services

Clinical Trial Monitoring

  • Oversee data collection
  • Review source documentation and case report forms
  • Ensure regulatory compliance
  • Resolve data queries
  • Conduct interim analyses as requested by clients
  • Risk based monitoring


Investigative Site Relations

  • Investigator meetings
  • Study communications


Continuous Quality Improvement

  • Business process re-engineering
  • SOP design, development, and re-engineering


Quality Assurance

  • Audit plan design and development
  • Clinical trial file and document audits
  • Investigational site audits
  • Vendor audits


Regulatory

  • Ministry of Health / Ethics Committee / IRB submissions
  • Regulatory compliance and document management