Our Clinical Trial Management team is a combination of qualified, trained and experienced Clinical Research, Regulatory Affairs and Quality Assurance experts. They provide high quality services in the following areas of Clinical Research for your drugs and medical devices;
- Study Design and Protocol writing and review
- CTA/IND and ITA/IDE Application preparation and submission with Health Canada and FDA
- Study Data Analysis and Report writing/review for regulatory submission
- Study Adverse Event management and reporting
- Study site monitoring and auditing
Feel free to contact us with your request for review and quote.