Start Up Fees
Regulatory
Site Costs
Hidden Traps
Often forgotten Line Items
100

This mandatory meeting occurs occurs before trial launch to train site investigators on protocol

What is an IM or SIV

100

This file tracks all the essential documents and requires dedicated archiving resources

What is the Investigator Site File or Trial Master File

100

This type of procedure-based site funding reimburses the site  for actual tests, labs and visits performed

What is activity-based or per-patient funding

100

This expensive event happens when a patient signs the consent form but fails to meet clinical eligibility

What is a screen fail

100

This fee is paid to ensure we maintain good relationships with our fellow sites

What is a referral fee

200

This start-up cost involves processing of regulatory documents and submitting them to the IRB

What is an Ethics Fee

200

This institution regulates research studies in Canada

What is Health Canada

200

This non-clinical percentage is added to every study budget to cover facility infrastructure

What is overhead (or Indirect cost)

200

Modifications to the Study Protocol during the study triggers these costly events

What are protocol amendment fees

200

These costs are used when ad hoc events occur or additional assessments are required

What is Invoiceable items

300

This line item allows for handling investigational product, accountability and requires dedicated budget allocation

What is the Pharmacy Set up fee

300

This entity holds a searchable database of all research trials

300

This staff member spends the most time on the study

Who is the Clinical Research Coordinator

300

This economic factor must be added to multi-year budgets to account for rising costs

What is inflation

300

This cost can easily be overlooked when a CT scan for assessment of AE, is required, and the CT is usually sent to a Central Vendor.

What is the local over-read and reporting cost

400

Negotiating this type of fee protects the site against losses when reviewing a patient database.

What is a pre-screening Fee

400

This entity holds the ultimate regulatory and data integrity of the study

Who is the Sponsor

400

This fee is charged to manage the review of regulatory and source documents

What is Monitoring Visit Fee

400

This factor should be added to Coordinator costs to account for operational costs

What is Employment Benefits

400

These items were an unexpected new cost during 2020 that had to be rapidly negotiated

What is PPE or COVID testing

500

What term is used for costs that are to be paid even when the contract is not executed.

What is Non-refundable cost

500

This version is the most recently Health Canada approved Good Clinical Practice Guideline

What is ICH E6(R3) 

500

This is the average increase % between intial budget from Sponsor and final 

What is 35%

500

This is a fee that is often insufficiently offered on inital budget and is a regulatory requirement by all academic institutions

What is archiving costs

500

This invoiceable item should be remembered in order to support new staff and returning staff

What is a retraining/reaccrediting fee