Drug Regulatory

We are providing global regulatory services to companies for the development and Registration of their products for their new chemical entities and biological. We support companies by preparing clinical development plans and regulatory strategies and further firming up these through pre-IND and scientific advice meetings.

We have well experienced staff in Regulatory Submission and Medical Subject Experts for Clinical Development plan.

• Product Registration
• Import License
• Market Authorization
• NRA Communications & Meetings
• Pharmacovigilance
• Test License
• Regulatory Documents review and submission
• Preparing Regulatory Development Plans