It does not work without YOUR input

 

Before a new medicinal product is introduced to the market, safety, efficacy and tolerability have to be tested. YOU have the experience with your product and we have the experience how to bring YOUR product to YOUR planned market.  

LaNova Consulting one step ahead
LaNova Consulting                             one step ahead
We appreciate the opportunity to demonstrate our capabilities as well as our intent to earn the trustworthiness and a longtime business relationship with your clients.
WE ARE .....
a Medical Research Consulting Company with a wide international active network in academia and industry to cover the research needs of Pharma, Biotech and MedDev. Companies as well as Health Care Associations.

 

 

WE OFFER .....

the following unique capabilities that allows LaNova Consulting to differentiate itself in Pharamcovigilance, Clinical Trials, Health Economics and Market Access in Europe and the GCC Region:

  • Phase II – IV Clinical Trials
    
  • Non Interventional Studies
    
  • Real World Evidence Evaluations
  • Investigator Initiated Trials
    
  • Pharmacovigilance Services
    
  • Medical Writing Services
    
  • Market Access Strategies to GCC
    
  • Consulting in Drug Development & Study Design
    
  • Consulting in Pharmacovigilance
    
  • Responsibilities as QP PV - § 63a AMG
    
  • Medical Advisory / Medical Affairs
    
  • Medical Management Consulting
  • Clinical Research Training (e.g. GCP, GPP) programs
    
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