Over 17 years of extensive global expertise
in preparation and execution of clinical trials

with medical devices and investigational drugs in different therapeutic areas
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RESPONSIBILITY

LG Medical Consulting

Extensive experience

Experience includes all phases of investigational drugs and both implantable and non-invasive medical device clinical trials, including but not limited to developing, training and supporting implant procedures, programming and troubleshooting, data collection and monitoring, as well as the support of sales activities.

Global Expertise

We are a dedicated team of experienced clinical research professionals, and our strategic location in Toronto, Canada, make us a valuable partner for companies across the globe conducting clinical trials in North America.

Professional Certifications

Our team members are Certified Clinical Research Professionals and Clinical Research Associates and hold advanced degrees in Health Sciences.

Services Provided by
LG Medical Consulting

Located in Toronto, Canada
  • Identification and initiation of investigator site
  • Protocol Training
  • Clinical Site Support and Management
  • Clinical Trial Monitoring: Pre-Study, Initiation, Interim, Close-out
  • Overseeing data collection
  • Ensuring regulatory and protocol compliance
  • Product Training to physicians, clinical staff & technicians
  • Technical Support for investigational device usage
  • Support of surgical procedures in OR and Cath Labs
  • Programming & Troubleshooting
  • Follow-up Tuning & Titration
  • Informed Consent Development & Review
  • Clinical Investigation Plan Development
  • Development & Review of Guidelines & SOPs
  • Ethics Committee Documents Preparation & Submission
  • Regulatory documentation maintenance