Product Registration

Pharmaceutical Products Registration
Biological & Biosimilar Registration
Medical Devices & IVD Registration
Cosmetics Registration
Food Supplements Registration
Disinfectants & Antiseptics Registration

Regulatory Submissions (CTD & eCTD)

CTD Dossier Preparation
eCTD Publishing & Submission

Quality & Compliance

Quality Management System (QMS)
GSDP Certification for Warehouses
QMS for Pharmacovigilance Offices
Audit & Compliance Readiness

Post-Marketing Vigilance

Pharmacovigilance Services
Medical Device Vigilance (Materiovigilance)

Training & Regulatory Consulting

Regulatory Affairs Consulting
Regulatory Affairs Training
CTD & eCTD Practical Training
GSDP & Quality Systems Training

Training & Programs Insights Contact Us Book

Your trusted partner for pharmaceutical regulatory affairs, product registration, quality systems, and regulatory consulting in Egypt and across the Arab region.

ISO 9001:2015 Certified · EGAC | IAF

Services

Product Registration
Regulatory Submissions (CTD & eCTD)
Quality & Compliance
Post-Marketing Vigilance
Training & Regulatory Consulting

Get In Touch

29 El-Ekhshid St., opposite El-Ekhshid Grand Mosque, Manial El-Rouda, Giza, Egypt 11555

© 2026 MS Web Development. All Rights Reserved.

Privacy Policy Terms

Services/Post-Marketing Vigilance/Medical Device Vigilance (Materiovigilance)

Post-Marketing Vigilance

Medical Device Vigilance (Materiovigilance)

Pharmacovigilance and materiovigilance systems and operations to ensure ongoing compliance and patient safety.

Request a Consultation Back to Post-Marketing Vigilance

Post-market systems and reporting

Timelines and compliance

Risk-based continuous improvement

Medical Device Vigilance (Materiovigilance)