CiPharma are the leading provider of life sciences professional services and training offering fully integrated solutions to help pharmaceutical manufacturers become more competitive and successful in today’s evolving market.

Drawing on our scientific, regulatory, and business expertise, CiPharma provides flexible, strategic solutions designed to fit your specific products, stage of development, and company size and goals.

CiPharma partner with biopharmaceutical and medical device companies to develop a streamlined, cost effective and customized approach focused on results, targeting those areas that represent the highest business and compliance risk. Part of what makes the CiPharma approach so effective is our ability to seamlessly blend in with your team. From systems, to processes, to operations, CiPharma provides a partner with a proven track record that will empower you to manage and improve your business performance providing expertise and training at every stage of the product life cycle, from inception through to patent retirement.

Key Benefits

  • Greatly reduce or eliminate the risk of non-compliance and the related costs and other business impacts
  • Improve reliability and efficiency of your processes throughout their life cycle
  • Increase availability and production throughput for your manufacturing facilities

Key Capabilities

  • Vendor/platform independent regulatory compliance, validation, consulting and integration services
  • Risk management, including regulatory compliance gap assessments, interpretation of regulations and compliance assessment of systems from sensor to boardroom
  • Project management planning, management, implementation and execution
  • Training of personnel, management and staff
  • Science-based Quality by Design (QbD) and Process Analytical Technology (PAT) project support
  • Legacy equipment 21 CFR Part 11/EU cGMP Annex11 compliance
  • Biotech process simulation