Registration

Device

Manage regulatory affairs portfolio by way of Regulatory Strategies, Feasibility Studies, Dossier compilation and filings, Agency follow ups and approvals, Post Approval License Management, Regulatory Compliance and Regulatory due diligence.

PharmSEA Counsultancy team is a niche scientific and regulatory consulting group. We guide and assist pharmaceutical, biotech and healthcare companies in the design and implementation of innovative and global regulatory strategies in order to expedite product development and registration of drugs, biologics, medical devices, combination products, and other healthcare products for all stages of development.

We are a team of experienced regulatory professionals, having rich experience in registration of pharmaceutical products and medical devices in the South East Asia, Africa and CIS regulatory environments who advise and provide regulatory support for products registration in all stages of development. We collaborate with companies to bring products to the market in the most efficient and cost-effective manner, within an evolving and increasingly challenging regulatory environment.