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    Jyton CRO Advantage
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Jyton CRO Advantage

 

l           Decade long experience with top medical device and biotechnology companies worldwide

l           Documentation as per international and Chinese standards

l           Excellent Communication

      - Weekly updates and status report

      - Online communication via Jyton SMARTman project management system

       - Close contacts with SFDA experts and PIs from most SFDA authorized clinical research sites.

       - Fluent English and Chinese communication

l           Frequent visits of client to Jyton sites

l           Routine audit by clients

l           Fully integrated service provider

l           Absolute assurance of intellectual property protection

l           Full quality management and GCPs

l           Deliver with international practices and guidance

l           Considerable experiences and knowledge of Chinese regulations and rules in full  

range of medical devices

l           Customized programs for various purpose including RA, marketing and R&D.

 

 

Jyton CRO is experienced in conducting complex, procedurally intensive clinical research. We offer:

 

(1) screen and decide PIs and hospitals

(2) Protocol design and consultation

(3) medical translation

(4) Source Documents Management

(5) Development of CRFs (cast report form) and establishment of e-CRFs??

(6) Organize investigator meetings

(7) EC submissions and approvals

(8) Sample management

(9) monitoring

(10) AE and SAE reporting and troubleshooting

(11) Data management and biostatistics

(12) Clinical reporting

 

 

 

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