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RTI-HS HomeOur ServicesDrug Safety and Pharmacovigilance › Medical Monitoring

Medical Monitoring

At RTI-HS medical monitoring is provided by licensed physicians who have extensive experience in clinical development and review of SAE and AE cases.

Comprehensive Services
Our medical monitors provide expert support throughout clinical development and post-marketing. Our medical monitoring services include:
  • Coverage by licensed physicians
  • Assessing subject eligibility
  • Evaluating study protocols and informed consents
  • Analyzing and reporting serious adverse events (SAEs)
  • Tracking participants’ safety throughout the trial
  • Assessing the benefits and risks on an ongoing basis
  • Identifying safety signals and safety trends

Related Services
Although medical monitoring can be a stand-alone service, we can also provide a custom proposal that will meet your unique needs by providing you with a suite of complementary services, including pharmacovigilance, biometrics, risk management, medical consulting and medical writing.

 


 
SENIOR LEADERSHIP

 
Maria Vazquez-Gragg, MD, MPM
Global Head, Safety and Pharmacovigilance


For a full list of scientific staff bios, click here.

 
DOWNLOADS

  Fact Sheets
- Pharmacovigilance
- Medical Monitoring
- Medical Consulting and
Writing
- Pharmacoepidemiology
- Therapeutic Risk Management

Other
FDA's Guidance for Industry:
- Good Pharmacovigilance Practices and Pharmacoepidemiologic Assessment

EMEA's Guidance
- Directive 2001/20/EC (Clinical Trial Directive of 4 April 2001)
- Pharmacovigilance for Medicinal Products for
Human Use


CONTACT US
To learn more about our research and consulting services, please call us at:
US: +1.800.262.3011
Spain: +34.93.241.7766
UK: +44(0)161.232.3400
Or email one of our experts directly.
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