ISAZI is a value driven private pharma and techno consulting company with its head office situated in Vadodara, India offering the highest quality regulatory services to the pharmaceutical companies worldwide. ISAZI is committed to step up your pharmaceutical business to the next level in terms of regulatory and compliance. Regulatory Services: Isazi provides regulatory services across all the spectrum of glob. We provide services related to New Product and Market Authorisations, Health Authority submissions, Post Approval Activity, Life Cycle Management, Regulatory Assessment, Health Authority Queries Responses and other regulatory activities. eCTD / publishing services: With expertise in Regulatory publishing services, we can help applicant to prepare electronic, eCTD, NeeS submission format. Regulatory labelling services: Labelling revision and maintenance of label requirement as per health authorities expectation is one of the most critical part in the pharma industry. We provide end-to-end solution for labelling requirements. Regulatory Software: Data fetching and maintaining is one of the biggest challenge in the pharma industries. We provide customised solution to this problem by proving customised software as per need. Project Management: Isazi provides project management support to ensure timely submission of the dossier to health agency. Quality and Compliance: We provide GxP Audit Services, QMS Remediation Services, Process and Product Validation and GxP Solution Consulting.