Understanding the Algerian Regulatory Framework
Algeria enforces strict regulatory standards for medical devices to protect public health and align with international best practices. Any medical device intended for commercialization must comply with national regulations and undergo evaluation by the competent authority.
Our expertise allows partners to navigate this complex process with confidence and efficiency.
Our Mission
Accurate classification is essential, as it impacts documentation requirements,review timelines, and approval procedures.
Industrial & Technical Support
Advanced MedPharma conducts in-depth quality audits aligned with ISO and GMP requirements to identify gaps and ensure compliance.
- System, product, and documentation audits
- Development and monitoring of CAPA (Corrective and Preventive Action) plans
- Delivery of expert compliance recommendations
Quality Audits (ISO & GMP)
Advanced MedPharma conducts in-depth quality audits aligned with ISO and GMP requirements to identify gaps and ensure compliance.
- System, product, and documentation audits
- Development and monitoring of CAPA (Corrective and Preventive Action) plans
- Delivery of expert compliance recommendations
Quality Assurance Systems
We design and implement complete Quality Assurance systems tailored to your operations and regulatory obligations.
- Design of QA processes and documentation frameworks
- Drafting of SOPs, stability protocols, and batch manufacturing records
- Alignment with international quality standards
Regulatory Affairs & Registration
Why Advanced MedPharma?
- Combination of strong technical expertise and regulatory mastery
- Focus on compliance, performance, and patient safety
- Simplified registration and production upgrade processes
Partner With Us
Secure regulatory excellence for your production units and accelerate your pharmaceutical development journey.
Partner with Advanced MedPharma today.
