Training Details: On February 25, 2021, CDSCO released a notice requesting all stakeholders involved in clinical trials for the online submission of SAE reports through the SUGAM portal (www.cdscoonline.gov.in) effective March 14, 2021. CDSCO also released a user manual and video tutorial on their website as a training aid which was timely and beneficial for the stakeholders.  
To further this training support and based on the feedback received from key stakeholders (Investigators and Site Staff), ISCR is happy to announce the development and release of simple & intuitive online training for the SUGAM Portal to train site staff from access, reporting, training documentation and troubleshooting perspective. 

This training can be accessed on demand and completed at the learner’s convenience. It will equip you to remain compliant with the regulatory requirement for SAE reporting. This online training will take approximately 1.5 hours to complete and does not require any specific software or application download. 

Once training is completed you will also receive a ‘’Certificate of Participation’’ from ISCR for the same. Registration Details- 
Please use the link for online registration below to register (or) You can also access www.ISCR.org and click the link available on the ICSR website to register.  

Once registration is complete and ISCR launches the training you will receive a welcome email from our LMS vendor with your login credentials. Use these credentials to log into the training, please keep you login details confidential and do not share.  
Please note that this training is being rolled out only for investigators and site staff who are currently conducting clinical trials in India and any non-site participants will not be provided access for the training.  

Registration Fees- None- Complimentary for our investigators and site staff. Registration will be for limited participants only and on first come first basis.  

ISCR is happy to announce that we have begun the Registrations for the Industry designed Self-paced Training and Certification Course for Clinical Research Coordinators! 

Clinical Research is evolving in the country as well as across the globe. One of the key stakeholder to conduct quality clinical research is the ‘Clinical Research Coordinator (CRC)’ and it is therefore essential to ensure that CRC is well-trained and able to assist the investigator for conduct of the relevant aspects of the trial.  
 

Indian Society for Clinical Research Announces-

Launch of Online Training for Ethics Committee ( EC) Members and Office Bearers  

Training for Safety Reporting/ Review via SUGAM Portal  

Registration Fees- None- Complimentary for our Ethics Committee members and Staff. Registration will be for limited participants only and on first come first basis.

Once registration is complete and ISCR launches the training you will receive a welcome email from our LMS vendor with your login credentials. Use these credentials to log into the training, please keep you login details confidential and do not share.

Please note that this training is being rolled out only for EC members and staff who are currently conducting clinical trials in India and any non-EC participants will not be provided access for this training.

Launch of Online Training for AMO Staff Involved in SAE Reporting and Processing

Indian Society for Clinical Research (ISCR) is happy to announce the launch of
‘Clinical Data Management-Certification Course’
with an Industry designed Self-paced and module driven training.