EDA GMP
Human & Veterinary
Liquid Dosage Forms
Fully equipped for the high-volume production of Syrups and Suspensions, with high-shear mixing, in-line homogenization and monoblock filling under GMP-classified environments.
- Syrups
- Suspensions
Plot 7183 · Sadat Industrial City · Egypt
Precision pharmaceutical manufacturing, engineered to GMP.
Advanced human and veterinary production lines built on strict compliance with current Good Manufacturing Practice (cGMP) standards — trusted by leading brands for powders, ointments, and syrups.
Confidential Inquiry
NDA-protected. Reply within 24h.
- GMP
- Certified
- High-Capacity
- Lines
- MENA Regional
- Routes
- 24/7
- QA Oversight
cGMP Compliant
In-house QC Lab
Regulatory Ready
NDA Protected
ABOUT US
Advanced Pharmaceutical Infrastructure Engineered for Global Excellence.
Strategically located in Sadat Industrial City, Alawael features cutting-edge, automated production lines designed to achieve maximum efficiency and strict quality compliance. From high-capacity formulation to precise batch packaging, our facility operates under rigorous cGMP environments to deliver flawless contract manufacturing solutions for both human and veterinary pharmaceutical brands.
Advanced HVAC & Controlled Environment Classification
Purified Water Systems & High-Performance Utilities
End-to-End Batch Traceability & Serialization
Dedicated Human & Veterinary Production Suites
EDA GMP
Certified
P-309/2026
Verified
Quality Authority
Fully certified by the Egyptian Drug Authority — under WHO guidelines.
Alawael operates under an official EDA GMP certificate aligned with World Health Organization manufacturing guidelines. Every production line, utility system, and quality process is qualified, documented, and re-validated on schedule — giving partners immediate confidence in every batch that leaves the site.
EDA GMP Certificate No.
P-309/2026
Issued by
Egyptian Drug Authority
under WHO guidelines
Valid until
April 30, 2028
Renewable
IQ / OQ / PQ
Rigorous Equipment & System Qualification
USP / EP
Strict Pharmacopeia Compendial Methods
Data Integrity
Absolute Alignment with ALCOA+ Principles
Production Lines · EDA Certified
Certified dosage forms under one GMP roof.
Manufacturing scope authorized under EDA GMP Certificate No. P-309/2026 — segregated human and veterinary production environments, each qualified and audit-ready.
EDA GMP
Human
Semisolid Dosage Forms
Advanced lines dedicated to manufacturing medical Creams and Ointments, with jacketed vacuum mixers and precision tube filling for consistent, contamination-free batches.
- Creams
- Ointments
EDA GMP
Veterinary
Solid Dosage Forms
Certified lines for specialized Powder formulations filled in sachets, plastic sachets, jars, metal cans, or paper bags — with dedicated dust-controlled powder-handling suites.
- Powders — sachets, jars, cans, paper bags
EDA GMP
All Dosage Lines
Packaging Capabilities
Full integration of certified Primary and Secondary packaging protocols across every dosage line — including labeling, cartoning, batch coding and serialization-ready workflows.
- Primary Packaging
- Secondary Packaging
Our Portfolio
Registered Pharmaceutical Products
4 EDA-registered veterinary products manufactured in-house under cGMP — Alawael-branded oral solutions and water-soluble powders for poultry and livestock.
VeterinaryOral SolutionRibospot
AlawaelVeterinary Oral Solution
500 mL·Antibiotics
Target: Veterinary use
EDA Reg. 5166/2021
VeterinaryPowder for Oral SolutionApratower
AlawaelApramycin Sulfate
800 mg/g·Antibiotics
Target: Pigs, Calves, Broilers
EDA Reg. 5173/2021
VeterinaryWater-Soluble PowderGallipoult
AlawaelWater-Soluble Powder
100 g·Antibiotics
Target: Poultry
EDA Reg. 4232/2018
VeterinaryWater-Soluble PowderLarofloroxal
AlawaelWater-Soluble Powder
100 g·Antibiotics
Target: Poultry
EDA Reg. 4241/2018
View all 4 products
Full dossiers and EDA certificates available on request under NDA.
Toll Manufacturing
Your Trusted Toll Manufacturing Partner
Facility-ready in Sadat City with regulatory-grade quality systems and scalable commercial volumes — engineered for third-party brands that will not compromise on compliance or continuity of supply.
Full GMP Compliance
The highest standards of quality assurance and disciplined technology transfer — audit-ready at every stage.
Flexible Batch Sizes
From pilot trials to full commercial scale runs across human and veterinary liquids, ointments, and powders—tailored perfectly to your market needs.
Confidentiality & NDA Secured
Every engagement begins with an NDA. Your formulas, IP and commercial plans stay fully protected.
Dedicated Partnership
A single-point technical account manager coordinates regulatory, production and logistics from day one.
Cooperation Process
A clear, four-step path from inquiry to commercial supply.
- 1Step 1
Inquiry & NDA Signing
First conversation, mutual NDA and scoping of your product portfolio.
- 2Step 2
Tech Transfer & Formula Evaluation
R&D review, feasibility, materials sourcing and process fit assessment.
- 3Step 3
Trial Batches & Stability Testing
Pilot manufacturing, ICH stability studies and analytical method transfer.
- 4Step 4
Commercial Production & Packaging
Full-scale GMP manufacturing, primary and secondary packaging, release.
Contact Us
Let's discuss your contract manufacturing project.
Share a few details about your product and volumes. A dedicated partnerships manager will follow up personally — typically within one business day.
Factory
Plot no. 7183, 7th Industrial Zone, Sadat City, Egypt.
Phone / WhatsApp
Phone / WhatsApp
Confidential Inquiry
Use the form at the top of the page to send an NDA-protected message.
Response Time
Our partnerships team replies within 24 business hours.
What to Include
Product type, target markets, estimated volumes, and preferred timeline.
NDA Protection
All project details are protected under strict Non-Disclosure Agreements.