Agency experience, boutique approach

Powered by a team with extensive regulatory agency experience at a European and national level,  including former agency reviewers, VCLS advises life sciences companies on effective strategies to develop early phase, innovative technologies, with the prospect of a long-term service to get their products to market. Strategies will provide the optimal regulatory, clinical and health economic pathways available.

Every client case is different and has its own particular needs. At VCLS, we act as the extension of your product development team and offer customized solutions. 

Integrated operations bridging over the Atlantic

Our experts in Europe and the US work within a project matrix team to provide our clients with coherent regulatory advice and strategies that cover the full range of development activities from preclinical development right the way through to marketing authorization and product lifecycle management.  The outputs provide a pathway suitable to navigate the FDA and EU agencies requirements.

Regulatory Strategy & Roadmaps

Global Regulatory Strategy & Roadmaps

  • Gap analysis
  • Integrated product development planning and execution
  • Product positioning
  • Regulatory pathway
  • Due diligence
  • Market Access Considerations
Regulatory Preparation & Submissions

Global Regulatory Preparation & Submissions

  • MAA (Centralized procedure, mutual recognition procedure, decentralized procedure) / NDA / BLA / IND
  • Clinical trial applications (INDs, CTAs, CTNs)
  • CE-marking technical files
  • Integration of HTA insights
Agency Interaction

Regulatory Agency Interaction

  • EMA, National  Scientific Advice
  • Pre-IND, EOP2 meetings, pre-NDA meetings
  • EMA SME meetings
  • ITF meetings
  • EMA/HTA parallel consultation
  • ODD
Lifecycle Management

Regulatory Lifecycle Management

  • Strategy and implementation
  • Post-approval lifecycle management including variations, amendments, renewals, supplements and annual reports


  • SME status
  • US agent
  • ODD sponsor

Have you thought about integrating value-based payer evidence requirements into your clinical development programs?

Discover more services at VCLS


Market Access