BlueReg Group Market Specific Services Page 3
Development Registration Commercialisation Market Specific Services Outsourcing Programs
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Market Specific Services

BlueReg has a dedicated team of experts who cover the whole development process from concept to approval, on centralised and multi-national projects.

 

Our consultants have diverse experience ranging from regulatory strategy to operational execution and full project management support will be provided.

We will provide a flexible approach designed to fully support your needs which will be adapted as the project evolves. All activities are carried out in compliance with local and regional regulatory requirements.

Your requirements for support and the time to engage with BlueReg

This service can be utilised during the entire registration process, through to launch and post marketing activities. BlueReg can guide you through the country to country requirements for local regulatory strategy, launch preparation, promotional copy review, healthcare compliance, pharmacovigilance, quality, supply chain, labelling review, pricing and reimbursement and post-approval submissions.

 

We provide local in-country resources and support as required.

 

Support is provided through our in-house team utilising, when required, the support of our qualified worldwide partner network who have significant national experience. BlueReg will provide full project management for all engagements from single market to multi-country / multi-regional projects with assignment of a designated project lead.

 

Our services can supplement client in-country resources or we can undertake all market activities on your behalf as required.

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Market Specific Component Services

Services provided by our team include:

 

  • Development strategy and advice
  • Interactions with regulatory agencies
  • Clinical Trial Applications (CTAs)
  • Scientific Advice (European Medicines Agency and national agencies)
  • Orphan Drug Designations (ODDs)
  • Paediatric Investigation Plans (PIPs)

 

 

 

  • Drug registration and registration strategy
  • Marketing Autorisation Application (MAA) dossier preparation
  • Post MAA regulatory maintenance
  • Regulatory publishing
  • Regulatory support
  • Local in-country support services and regulatory support

“It is really incredible, how perfectly all has worked out, and we found for all challenges pragmatic but fully compliant solutions. This is extraordinary and an excelling result, we all can be very proud of.”

Associated services

We provide local in-country resources and centralised regulatory support, as required, for all manner of market specific services.
Support is provided through our in-house team utilising, when required, the support of our qualified Global Partner Network who have significant national experience. BlueReg provides full project management for all engagements from single market to multi-country / multi-regional projects with assignment of a designated project lead.

Latin America Team