OUR UNWAVERING COMMITMENT
<h2 class="dsvy-element-title">Quality Management</h2>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.
Department of Pharmacovigilance
<h2 class="dsvy-element-title">REPORTING ADVERSE DRUG REACTIONS</h2>How to RAD
Importance of Early Reporting
Recognizing Symptoms
Healthcare Communication
Impact of Adverse Reactions
Preventive Measures
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
Below are the reporting forms.
Paper Forms
- RAD
- RPQ
- RAE
Download the form to report any drug interactions and help us ensure patient safety.
Download the form to report any product quality issues and help us maintain high standards.
Download the form to report any adverse events and help us improve our pharmaceutical products.
Contact an expert
Download the SBDMA application
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.
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.