At Medilife we can offer a ‘Rescue Package’ that enables a swift change. We start by evaluating your current documentation, status and obtaining feedback from KOLs and research teams to provide honest and transparent feedback on how to improve the trial before committing to deliverables that we are certain of being able to deliver.

Benefits:

• Current documentation and status review

• Independent gathering of feedback

• Assessment of opportunities to improve study recruitment

• Re-baseline of recruitment expectations including risk management

• Payment structure based on milestones and deliverables

Includes:

• Independent assessment of current clinical trial health

• Current documentation and status review

• KOL feedback

• Re-baseline recruitment plan

• Risk Mitigation and enrolment boosting strategies

• Rescue recommendation written into report

From £6,500

Utilising our regulatory experts, we can provide a study set up package that includes obtaining regulatory approvals, writing clinical study documentation, site set up and budget and contract negotiations. 

Benefits:

• Accelerates Clinical study start

• Ensures clinical study set up moves forward whilst resourcing gaps are filled

• Utilising our expert knowledge and procedures with no obligation for clinical study execution

Includes:

• Accelerate study start up

• Obtain regulatory approvals

• Writing of clinical study documentation

• Site set up

• Site budget and contract negotiations

• Utilize Medilife SOPs

• Avoid delays whilst resource gaps are filled

From £21,500

We can utilise our network of trusted sites to conduct site feasibility and selection on your behalf for a fixed fee. 

Benefits:

• Ensures clinical study set up moves forward whilst resourcing gaps are filled (e.g. hiring or working on protocol development). 

• Medilife work alongside your existing team to understand the requirements

• Quick site selection based on existing relationships and experience

• Utilising Medilife’s SOPs and procedures

• Trusted site partnerships to propel study forward

Includes:

• Selection of UK sites within our expert therapeutic area

• Feasibility survey development and assessment of interest from sites

• Site selection visits

• Useful for ensuring clinical set up moves forward whilst resourcing gaps are filled

• Quick movement due to existing relationships in country

• Utilize Medilife’s SOPs

• Trusted site partnerships to propel study forward

From £12,500

• Site identified by Sponsor

• Utilizing Medilife’s SOPs and expertise

• Includes CRA training time

From £3,500

• Obtain ethics approval for Medical device study utilizing your study documentation

• Review of current trial documentation to ensure requirements are met

• Submit ethics application using Medilife SOPs

From £7,000

• Obtain MHRA approval for Medical device study utilizing your study documentation

• Review of current trial documentation to ensure requirements are met

• Submit ethics application using Medilife SOPs

From £9,000

• Taking current protocol and essential documents, writing supporting manuals for clinical trial execution e.g Monitoring plan, project management plan, data management plan

• Utilize Medilife Templates

From £3,000