We provide technical guidance and support for project management right from its inception for Phase I-IV drug trials and device studies, which include protocol development, medical writing, literature review, monitoring and coordination, communication, follow-up with regulatory authorities, IRB/ IEC, Pharmaco-vigilance, Clinical Research Training.
Maintaining the safety and efficacy issues on the forefront, and following the guidelines of ICH and GCP and appropriate guidelines/ SOPs and protocol, we are committed to serve the humanity to improve global health. With the expert, efficient and experienced pool of resources we undertake following responsibilities: |