- Adverse Event reporting has increased substantially in the last few years.
- Clients and CRO’s are both looking to reduce costs and increase efficiencies.
- Intense scrutiny of medical devices by regulatory authorities (EU-MDR and FDA) increasing both in Europe and US.
- High quality data driven clinical research, ISO...
- The pharmacovigilance industry is poised for a quantum growth in 2020
- Complexities are increasing due to new drug launches and higher degree of regulatory requirements.