Services
Helping Your Medicines Reach the World, Safely & Smoothly
Regulatory Approvals and Affairs
Ashab Group helps pharmaceutical companies secure global approvals and maintain compliance through inspections, audits, and gap analyses, while expertly preparing and submitting regulatory dossiers and documents for key international markets.
Regulatory Affairs
Prepare, review, and submit complex dossiers and reports for approvals in key international markets
Business Acquisition Procedure
Prepare, review, and submit complex dossiers and reports for approvals in key international markets.
Europe Submission Services
End-to-end support for EU marketing authorization, QP services, pharmacovigilance, and product batch release/testing.
Technology Transfer
Transfer products and processes using R&D and EU dossier expertise to speed market entry.
Medical Devices
Regulatory, clinical, and compliance support for pharmaceutical medical device manufacturers.
Toxicology Services
Risk assessments, safety studies, and biocompatibility evaluations for pharmaceuticals, devices, and cosmetics.
Trading & Export:
Compliant global trading and export of pharmaceutical and Ayurvedic products with complete documentation and logistics support.