PLANT FACILITY

APEX Pharma inaugurated its state-of-the-art manufacturing site in 2005, located in Badr City, Cairo.

The manufacturing facility is constructed according to the cGMP guidelines to fulfill all the local and international regulatory standards including ISO, EU, WHO and FDA requirements.
For APEX Pharma, our key for continuous development of top quality products is identifying patients’ needs & ensuring that our staff are equipped with the skills, technology, and knowledge required to meet them.
Machines, equipment, services and processes had been validated in compliance with the latest updates of cGMP guidelines.
APEX Pharma has invested in the latest validated European equipments for solid, semisolid & syrup forms.
Apex Pharma is approved by SFDA (Saudi Food and Drug Authority) for the manufacturing of tablet, capsule, liquid & semisolid forms for internal use decree no.38/SFDA/926/27.
The atmosphere at the plant encourages a rich mix of integrity, individual creativity & collaborative sharing, allowing the best idea to manifest and leading to a continuous cycle of improvement.

PLANT SURFACE AREA

The total area of the factory land is 57,551 m2 and the built-up area is 14,000 m2 as follows:

Manufacturing Area

4000 m2

Warehouse Area

4800 m2

Administration Building

1800 m2

Utilities

1600 m2

New Extension

2200 m2

PLANT FACILITY
DEPARTMENTS

Our excellence in manufacturing top quality products is the yield of the integration of strenuous efforts exerted by different functions and departments. Below is a brief about the role of each department in our plant facility.

PLANT FACILITY
DEPARTMENTS

Our excellence in manufacturing top quality products is the yield of the integration of strenuous efforts exerted by different functions and departments. Below is a brief about the role of each department in our plant facility.

PRODUCTION

The core business function is turning primary starting inputs into valuable outputs through a series of processes.

DISPENSING

PREPERATION

FILLING

PACKAGING

Apex Pharma produces pharmaceutical products for human use including solid (tablet, capsule), semi-solid (ointment, gels, creams and suppositories) and liquid dosage form.

QUALITY CONTROL

Quality control refers to the sum of all procedures undertaken to ensure the identity,
purity & safety of a pharmaceutical product as per standard specifications.
Analysis of the starting materials, in-process sampling, finished products and environmental monitoring.

REASEARCH &
DEVELOPMENT

Study the feasibility of proposed new products.
Design and development of new products under registration in the company pipeline.
Verification and validation of new products design.
Development and optimization of the product Know how.
Scale up and transfer of the manufacturing process to production.
Provide data and technical documents related to new products registration.
Assist in technical troubleshooting of running products.

WAREHOUSE

The warehouse contains 2 main stores, one for the chemicals and packaging materials with storage capacity of about 6600 storage locations, and the other one for the finished products with about 2600 locations. In addition of some special stores for hard gelatin capsules, solvents, narcotics and consumables.

All warehouse functions are managed by the SAP system that offers the best technology for easy and fast transactions, and also gives a very powerful tracking and reporting tool to control the stock.

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