Clinical Data Management

At GK ANALYTICS we believe in providing high quality clinical data management to support your drug development needs to get drugs to market as quickly as possible so patients have access to drugs. We provide bespoke solutions tailored to your requirements and provide real time, faster access to data meaning faster decisions can be made to keep patients as safe as possible.

Our expertise allows us to focus solely on the data of a clinical trial and enables us to develop trust with long lasting partnerships. By concentrating exclusively on data we are able to offer efficient and flexible clinical data management services, we are seen as a niche provider for smaller teams or a valuable experienced partner for larger accounts.

GK ANALYTICS provides end to end comprehensive clinical data management services from Phase I through to post-marketing trials. Our team of global clinical data management experts are committed to upholding a standardized, process-driven approach.

Our Clinical Data Management Services include:


● On-shore and off-shore Clinical Data Management Services
● EDC and Paper Trial Set-Up & Management
● Certified Medidata RAVE Builders
● Access to other EDC solutions (Low Cost, Oracle etc.)
● Data Management Plan (DMP) development
● Data Management Project Management
● CRF/eCRF design and development
● CRF Annotation & Review
● Database Build & Design
● Data validation specifications
● Edit checks Programming & Testing
● Data processing through double data entry
● Query Management
● Medical Coding
● Safety Data Management & Reconciliation
● Data Export/Transfer
● CDASH Compliant deliverables
● Real-time data viewing and reporting

The key to a successful working relationship and part of our customer excellence approach with our clients is being flexible to their requirements. Therefore, our Lead Clinical Data Managers will work with our partner customers to define specific requirements and expectations to meet the partnership objectives .

Looking for a partner that can provide access to experienced leads and a cost effective solution to support your pipeline?

With tightening budgets in clinical research and development it can be a challenge to find solutions that provide access to expert knowledge and still meet the budgets that have been approved. Typical challenges include managing overheads on internal resource, dealing with the highs and lows of work in your pipeline and not having enough experts available in-house or via partners to handle, process and provide input into the clinical data. These are all typical challenges that we have developed solutions to help resolve..