We support local pharmaceutical cos for Bioequivalent Study for Semi-regulated & Regulated Markets.
We help local interested pharmaceutical company having UK MHRA to launch their own branded product to UK market.
We organize for technical training for pharmaceutical professionals
We are connected with a reputed organizations having decades of experience and expertise in gap analysis / pre-audit/pre-qualification of your facility.
We prepare dossier all types of dossiers i.e. ACTD, CTD & eCTD. We work for US/ANDA submission also.
Based on our customer demand, we help to purchase ready EU CTD / MA and to launch their own branded product to UK market.
We are connected with no of reputed consultants for API Turkey projects.
We do consultancy for setting up new project development such as MDI, Oncology, Biotech, Hormone, Insulin, API facility etc. We also do new project assessment, Project profile development etc.
We assist in establishing Quality Management System as per International Regulatory guidelines i.e. USFDA, UK-MHRA, EU-GMP, PICs.
We refer reputed imported brands for local marketing.
We are also, supporting our customers for tech transfer and contract manufacturing of API / imported products.
We also help to do in-lisencing & out-lisencing activitiy as per customer need.