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Primary contact

First Name

Last Name

Job Title

Company Name

Email

Phone Number

Company address

Street Address

City

State/Region/Province

Postal/Zip Code

Country

Company Type

Project scope

Study Name

Sponsor Name

Therapeutic Area

Indication

Study Phase

Estimated Duration of Study (in months)

Estimated Start Date

Number of sites

Number of patient screened

Number of patient randomised

Number of patient completed

Number of countries

Total number of CRF pages

Number of unique CRF pages

CRF Type
 Paper CRF eCRF Hybrid Model

Service Required

Data Management

 Data management/cleaning/coding

CRF Design
 Yes No

Laboratory Data Imports
 Yes No

 Patient Diaries

Statistic

 Statistical Consultancy

 Statistical Programming

 Statistical Analysis

 Statistical Analysis Plan

Randomisation
 Paper IWRS IVRS

Pharmacovigilance

 Case Processing

 Safety Reporting

 Medical Monitoring

 SAE Reconciliation

Medical Writing

 Clinical Study Report Writing

 Protocol Writing

Other

Consultancy

 Protocol Development

 Statistical Consultancy

 CDISC Consultancy & Support

Technology Support

 EDC

 ePRO

 Pharmacovigilance System

 IVRS/IWRS

 CTMS

 ERP System

 eLearning

 Helpdesk

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