Europe Pharmacovigilance and Drug Safety Software Market Forecast, Regional Share and Growth Opportunity Analysis to 2031
ArisEurope, ICON, Syneos Health, Accenture, IQVIA, Genpact, Cognizant, Paraxel International, Laboratory Corporation of ...
Medscape2d
Clinical Perspectives in Drug Safety and Adverse Drug Reactions
Spontaneous reporting continues to play an important role in pharmacovigilance and the value of astute clinical observation and well-documented reports of suspicions of a causal link cannot be ...
Armed robbery in Revesby1d
Solensia 7 Mg/ml Injection Solution for Cats
VMD response to concerns raised following media reports of serious adverse events in cats administered Solensia. The VMD is aware of media reports and ...
Pharm Exec1d
EVERSANA Partners with Lyfegen to Bring AI to Drug Pricing and Market Access
Many companies and investors believe that AI has to potential to reshape various elements of the pharma industry. Two ...
Euro Weekly News6d
Paracetamol risk: EU watchdog demands urgent review over new side effect
Paracetamol, now comes with a shocking new warning: it could lead to a dangerous condition called metabolic acidosis if ...
pharmaphorum4d
Keeping local affiliates on track with pharmacovigilance
These demands place companies at risk of falling foul of regulatory compliance requirements, particularly in pharmacovigilance (PV), given the importance of patient safety. What makes this highly ...
American Association of Individual Investors3d
Which Is a Better Investment, Bio-Rad Laboratories, Inc. or Medpace Holdings, Inc. Stock?
Learn more about whether Bio-Rad Laboratories, Inc. or Medpace Holdings, Inc. is a better investment based on AAII's A+ ...
pharmaphorum4d
Optimisation of signal management in pharmacovigilance
Module IX of the EMA’s Good Pharmacovigilance Practices (GVP ... Review of adverse event data and other important safety information is an important step in the assessment of a potential ...
JD Supra1d
FDA Publishes Its First Draft Guidance On Use of Artificial Intelligence in the Development of Drugs and Biological Products
On January 7, 2025, the FDA issued a draft guidance called Considerations for the Use of Artificial Intelligence to Support Regulatory ...
scientific-computing1d
Process optimisation and technology transfer
“So, we need to increase efficiency on the process development side. While automation is one way of doing that, a much more efficient solution is to use in silico process development data to increase ...