London, UK: +44 (0)333 332 1882 | Cambridge, Massachusetts: 617-674-2650 | San Mateo, California: 650-378-1270

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Patient Safety
 

To ensure compliance with evolving global and European regulations in various areas of drug safety, we offer solutions in:

  • Safety reporting in clinical trials 

  • Risk management and Periodic Reporting 

  • Pharmacovigilance Database: Data Entry, Medical Review and Expedited Reporting 

  • QPPV and pharmacovigilance systems

The scope spreads from ad hoc consultancy on scientific or operational aspects to packaged solutions, crafted to your specific circumstance. Please click here for more information




Clinical Development
 

Regardless how early you are in pre-clinical explorations or late in clinical drug development, we will help you maximise the value of your compound. Our main areas of expertise are:

  • Translational Science
  • Clinical Science 
  • Medical Writing

We can optimise your clinical development program to demonstrate clinical value based on budgetary and time constrains, advise on clinical trial design, and support you throughout your progress. 




 


Marketing Strategy and Medical Affairs 

We believe that it is never too early or too late to make sure that your products are set to maximize return on investment. We specialize in the following areas:

  • Assessment of commercialization potential
  • Development of Marketing Plans
  • Training of personnel 
  • Patient interactions

Our marketing plan will leverage clinical data, regional commercial micro- and macroenvironment, competition and regulatory environment to support your strategic targets.