As a full-service CRO, ProClin Research has an entire team of regulatory professionals to handle all the necessary regulatory submissions for clinical trials and product approvals. Ensuring a seamless end-to-end process, we will work directly with your team to develop the required materials, submit to DCGI and other regulatory boards on your behalf, and handle all correspondence until approvals are received.
Our team of regulatory experts, led by a former Regulatory professionals with the DCGI, is available to provide consulting throughout the clinical trial process. With a full offering of regulatory services, ProClin Research can also be contracted to submit to a regulatory board on your behalf for a clinical trial being run at an outside site or to obtain product approvals.