Our Services

We take care of your success

Contracts management

 

Negotiating contracts with Investigators

Managing the contract (amendments, appendixes)

Preparing and collecting up to date documents

Acting on behalf of the Sponsor

Professional

events

Organizing the venues

Inviting Investigators, Study Coordinators, CRAs and Vendors

Preparing training schedules

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Site set up

 

Preparing the route map for selected sites

Planning study milestones

Working on SOPs

Training site staff

Collecting all necessary documents

Vendors management

 

Selecting Vendors

Evaluating the services

Negotiating the collaboration agreements

Representing the Sponsor in every day contacts with Vendors

Clinical monitoring

 

Our monitors conduct all types of visits onsite and remotely:

  • Site evaluation visits

  • Site initiations visits

  • Interim monitoring visits

  • Closeout visits

CRF design

Designing CRF

Working on a paper and electronic version of CRF

Preparing tailor made eCRF

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Feasibility

Evaluating and selecting sites

Assessing Investigators

Assessing the capacity to conduct clinical trials

Investigating enrollment and retention rate in similar studies

Audits and QA/QC services

 

Clinical Trials Audits

Pharmacy audits

Inspection Readiness Visits

Assisting while MHRA Inspections

Regulatory

 

Being up to date with regulatory requirements

Preparing documents

Submitting country specific documents to EC

CROPRIME Ltd © 2018

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If you have any further questions please get in touch with us.

                                     +44 7711 108 352      |   Tel: +44(0)24 7659 3061    |   Croprime Ltd, 19 Trimpley Drive, CV6 3LJ Coventry