The department consists of three branches: the study of real stability, long and fast.
The department is concerned with the study of the stability of the developed pharmaceutical
products as well as the study of stability of production products in different storage
and for certain periods according to the latest international legislations related to the
nurseries and modern devices and intelligent follow-up systems.
Preparing product follow-up files to ensure that they do not depart from international and
local standards in preparation for registering products in the relevant authorities.
Department of Methods Development Analysis
The department performs its activities through the laboratory of chemical analysis,
physical analysis, microbiological analysis.
The department applies the methods of analysis adopted in the international product
constitutions (if any), develops new methods of analysis of unconstitutional products, and
conducts a feasibility study to ensure that they work properly for the purpose for which
they are based.
The department studies the bioequivalence in the laboratory of the drug developed in
comparison to the innovative drug according to the relevant scientific guidelines
The department uses these methods to analyze products during the development of the product
in the initial testing phase and during the stability study and then transferred to the
quality control department to be used to analyze the pharmaceutical product in the
Development of pharmaceutical formula
The laboratory consists of several laboratories: liquid drink laboratory, semi-solid
product laboratory (ointment, creams, gels and suppositories), solid product laboratories
(tablets and capsules), equipped with state-of-the-art medical equipment and equipment.
The department develops a generic drug that conforms to international standards. The
generic drug is developed from the collection of physical, pharmacological and clinical
information through preliminary experiments to the final version to meet the scientific and
international requirements, then to prepare meals to study consistency and transfer the
technology of the product from R & Production by supervising the first three production
meals as well as training on how to produce the product. The department participates in the
qualification of suppliers through conducting experiments on raw materials to ascertain the
extent to which they conform to internationally approved standards.
The department also contributes to the community through the training of pharmaceutical
staff in public and private universities. The department contributes to research related to
the study of the master's and doctoral students from different universities.
Knowledge Corner Unit
The unit consists of a corner equipped with the latest equipment of the Apple connected to
the Internet dedicated to research and reading room and a special training and workshops.
The unit aims to provide the center with all the modern knowledge related to the
pharmaceutical industry and the new updates related to the approved pharmaceutical
legislations worldwide and how to apply them through training programs and lectures.