IRB Services
- Central and Local IRB Services
- Experienced, CIP Certified Staff
- On-Site, Full-Time Medical Director
- Canadian REB Services
- Seasoned and Diverse Board
- Board Meetings Twice Weekly
- Assistance with Document Development, including:
- Informed Consent Development
- Protocol Development
- Draft protocol review and comment
- Certified Translation Services
Client Services
- Courteous and Attentive Staff
- Single Point of Contact for Study Duration
- Pre-Study Teleconferences
- Timely and Prompt Turn Around
- 3-5 Business Day Turn Around (Expedited Review) from date of submission
- 7-10 Business Day Turn Around (Full Board Review) from date of submission
- Notification Within 24 hours of Study Approval by Phone or E-mail (upon request)
- Accept all submissions via E-Mail, Facsimile or Mail
- Timely Communication
- Flexible Scheduling
|
Experience
- Phase I-IV studies in all Therapeutic Areas
- Extensive Phase I & Single Site experience
- Federally Funded Studies
- Multicenter Studies
- Unlimited Number of Sites
- Late Phase Studies - Post Market & Registries
- Device Studies
- Biologic Studies
- Nutraceutical Studies
- Cosmetic Studies
Web Tools
- A.S.A.P (Aspire's Simple Automated Portal)
- Web Portal access to view and download documents
- Online status updates
- 24/7 access
- Documents are posted to A.S.A.P. within 24 hours of approval
|
