+30
Year of Experience
+100
Regulatory Files Reviewed
+5
Government & Private Sector Leadership Roles
About Me
I’m Hind Ibrahim
A pharmacist and regulatory affairs expert with over 30 years of experience across the public and private healthcare sectors. My journey has taken me from clinical pharmacy in top Iraqi hospitals to leading regulatory efforts for global pharmaceutical companies.
I specialize in pharmaceutical registration, regulatory consultancy, and compliance, with a deep understanding of Iraqi Ministry of Health procedures and international standards. Throughout my career, I have successfully led regulatory departments, managed complex product registrations, and consulted for global companies like CEDEM AG – Switzerland and Global MATCH.
Known for my integrity, commitment, and problem-solving skills, I thrive in roles that require diplomacy, scientific precision, and strategic thinking. I’m passionate about creating pathways for innovative health solutions to reach the people who need them most.
Core Competencies
With a solid foundation in pharmacy and decades of hands-on regulatory experience, I bring a results-driven approach to pharmaceutical compliance. My work bridges scientific integrity with strategic planning, ensuring smooth product registrations and strong collaboration with health authorities.
Regulatory Affairs Strategy
Over 30 years of experience navigating pharmaceutical and supplement registration in Iraq.
Dossier Preparation & Review
Skilled in compiling, reviewing, and correcting technical files for MOH approval.
Compliance & Consultancy
Advising international companies on local regulatory requirements and procedures.
Authority Liaison
Proven track record in communicating with the Iraqi MOH and regulatory bodies.
Scientific File Evaluation
Strong background in analyzing clinical studies and product data for compliance.
Product & Company Registration
Expert in managing registration for pharmaceuticals, medical devices, and companies.
Skills
The Secret of Success
With decades of experience in regulatory affairs, I’ve developed a strong set of practical and strategic skills that support smooth product approvals and efficient collaboration with local and international partners.
Gap Analysis
Identifying regulatory deficiencies and aligning submissions with MOH requirements.
Registration File
Compiling and reviewing high-quality CTD/eCTD dossiers.
Sourcing
Connecting with trusted manufacturers and suppliers to meet market needs.
Regulatory Troubleshooting
ackling complex challenges with smart, compliant, and timely solutions.
Organizations I’ve Worked With
Throughout my career, I’ve had the privilege of working with respected organizations across the pharmaceutical and regulatory landscape, contributing to national healthcare systems and global partnerships.
Played a leading role in pharmaceutical product evaluation, company registration, and regulatory committee leadership at the national level.
Iraqi Ministry of Health (MOH)
Managed company and product registration, liaised with the MOH, and led regulatory file reviews.
Al Qand Company
Served as a senior regulatory consultant, guiding product registration and compliance for both pharmaceuticals and supplements.
Sawa Company
Currently serving as the Regulatory Affairs Consultant for Iraq, handling product approvals, private labeling, and strategic regulatory planning.
CEDEM AG
Latest news
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