Services

IIR Support

If you are an Investigator and you have an idea for a multinational clinical study, EVICR.net helps you to develop your idea in a clinical research study in ophthalmology. To submit your IIR proposal to the EVICR.net... more

Scientific advice including contributions to study design

EVICR.net is able to provide the scientific advice needed, including contributions to clinical trial design, particularly on the following areas of expertise: Age-Related Macular Degeneration Retinal Dystrophies... more

Certified Clinical Sites with harmonised procedures (SOPs), quality control and qualified personnel

The Clinical Site, once a Member of the network, receives 6 organisational Standard Operating Procedures (SOPs) to be adopted/harmonised with the help of EVICR.net Coordinating Centre in order to become a certified Clinical Site... more

Feasibility assessment for Clinical Sites participation and recruitment (performed at short notice)

A feasibility assessment includes strategic, scientific, operational and patient recruitment considerations, determinant for the success of the clinical study recruitment commitments in a timely and effective manner. EVICR.net... more

Administrative setup of contracts with Clinical Sites

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Help in achieving recruitment rate by contacting directly and regularly the participating centres

EVICR.net is able to help in achieving recruitment rate by contacting directly and regularly the participating Clinical Sites, identifying useful tools and strategies to improve recruitment rate. Need nursing essay writing help?... more

Certification and training of technical personnel

EVICR.net has collaborated with industry in specific activities for the certification of technicians and this way contributes to the implementation of a clinical study in Europe. If you have any need in this area please... more

Certification and training of technical personnel

EVICR.net has collaborated with industry in specific activities for the certification of technicians and this way contributes to the implementation of a clinical study in Europe. If you have any need in this area please... more