Data Management Clinical Data Management

Clinical Data Management is broken into very specific key tasks and all of them need to be managed by a Lead Data Manager. This individual will be the single point of contact for all your Clinical Data Management needs.

We have defined metrics and turnaround times for each step of our processes from database build and entry to query resolution and QC. This allows us to efficiently manage our time and ensure we provide you with accurate costs at the beginning of any study, which minimises change orders during the study.

We have a standard set of reports available that will detail each aspect of the data processing. These can be sent as regularly as required to allow productive meetings, especially towards database lock.

Our dedicated CRF design team use Indesign to create Case Report Forms, Source documentation, Diaries and Urinalysis booklets. Each CRF is based on our RPL standard library of CRF modules (in accordance with CDISC). However Richmond Pharmacology will modify or create CRF’s in accordance with your needs to ensure you receive the module you specifically require.

CRF instructions are prepared alongside the design of the CRF to ensure site staff are very clear on how to complete the required pages. These can be incorporated into the document itself or be a standalone document.

We pride ourselves on our rigorous QC processes producing a 0% error rate on critical items and less than 0.05% errors for all other data.

Contact Richmond Pharmacology for a full list of data management services

Case studies

The thorough approach to QTc studies ("Your perfect partner for conducting definitive thorough QT studies, all under one roof")

Timelines, Tight Timelines and Even Tighter Timelines in a Phase I Environment (We know we can help your business. We always rise to the challenge)