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OUR UNWAVERING COMMITMENT

Quality Management

At Enopharm, we view quality as an ongoing journey rather than a final destination.

As a premier pharmaceutical importer in Yemen, we are steadfast in our commitment to providing high-quality medicines that adhere to the strictest international standards.

Our robust Quality Management system covers every aspect of our operations, from selecting suppliers to storage and distribution.

This guarantees that every medicine we offer is safe, effective, and reliable.

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Our work process

Our Comprehensive Approach to Quality

At our Enopharm, quality is not just a goal; it’s a commitment. Our comprehensive approach to quality ensures that every step of our work process is meticulously planned and executed to meet the highest standards. From initial concept to final delivery,
Rigorous Supplier Selectio

Rigorous Supplier Selectio

Comprehensive SOPs

Comprehensive SOPs

Optimal Storage and Distribution

Optimal Storage and Distribution

Department of Pharmacovigilance

REPORTING ADVERSE DRUG REACTIONS

How to RAD

A step-by-step guide to reporting adverse drug reactions.

Importance of Early Reporting

Why early reporting of adverse reactions is crucial for patient safety

Recognizing Symptoms

How to identify common and rare side effects of medications.
Reporting

Healthcare Communication

The importance of discussing any adverse reactions with healthcare professionals.

Impact of Adverse Reactions

How adverse drug reactions can affect overall health.

Preventive Measures

Tips and guidelines to avoid adverse drug reactions in the future.

Importance of Reporting Adverse Drug Reactions

Reporting adverse drug reactions (ADRs) is crucial for ensuring the safety and efficacy of medications. By reporting any unexpected or harmful effects, healthcare professionals and patients contribute to a safer healthcare system. This information helps regulatory authorities and pharmaceutical companies to monitor drug safety, identify potential risks, and take necessary actions to protect public health.

Electronic Reporting

Electronic Reporting

You can report ADRs online through our secure electronic reporting system.
Go to the Reporting page

Below are the reporting forms.

Paper Forms

If you prefer, you can fill out a paper form available on our website. Detailed instructions on how to complete and submit the form are provided.

Your participation in reporting adverse drug reactions is vital for maintaining drug safety and improving patient care. Thank you for your cooperation.

The Role of Pharmacovigilance

Pharmacovigilance helps detect new or rare drug side effects, better assess drug risks and benefits, and improve patient safety by regulating medicine use and reporting adverse effects.
  • RAD
  • RPQ
  • RAE
RAD

Report Drug Interaction

RAD-1
Download the form to report any drug interactions and help us ensure patient safety.

RPQ

Report Product Quality

RAD-2
Download the form to report any product quality issues and help us maintain high standards.

RAE

Report Adverse Event

RAD-3
Download the form to report any adverse events and help us improve our pharmaceutical products.

Contact an expert

    Download the SBDMA application

    Report easily by downloading the SBDMA Pharmacovigilance app.

    Leading the Way in Drug Safety

    We maintain a comprehensive set of Standard Operating Procedures (SOPs) that meticulously outline every step of our quality control process. These SOPs are based on international best practices and Yemeni regulations, ensuring consistency and compliance.

    Go to the FAQ page

    We have a multi-step supplier selection process that involves thorough due diligence, quality audits, and regulatory compliance checks. We only partner with suppliers who meet our stringent quality standards and share our commitment to ethical practices.

    We actively seek feedback from various stakeholders, including employees, partners, and regulatory authorities, to identify potential areas for improvement. We also conduct regular internal audits and reviews to identify gaps and implement corrective actions. Additionally, we encourage employee participation in quality improvement initiatives and invest in ongoing training to enhance their knowledge and skills.

    We maintain a secure and accessible digital repository for all quality-related documents, including SOPs, the Quality Management System Manual, and the Quality Policy. This ensures authorized personnel have immediate access to the latest versions and facilitates efficient auditing and review processes.

    Quality Management: Excellence in Every Step 1