About Us
  • Who We Are
  • Site Master File
Who We Are
  • Cosmopack is one of the leading pharmaceuticals and cosmoceutical producers that has been established since 1962.
  • Operating under the provisions of the ministry of health in Egypt
  • Cosmopack’s products have been known locally and throughout the MENA region as a part of the company’s export strategy
  • The only distributer for our brands in EGYPT is ARTEV EGYPT FOR MARKETING AND TRADE
  • Our products known under the name of (logos of products ) in addition to other products being manufactured and packaged at our premises for our clients
  • Cosmopack is also has the ability of manufacturing cosmetics under company’s brand names or for a private label
  • Now adays and after expanding cosmopack’s plan ,our facilities accommodate production lines for hair products including hair straightening and hair care , skin care products , and baby care
  • Our portfolio consists of over 300 products being produced and packaged at our facilities being traded under the brand name of the local distributers
  • cosmopack got certificates ISO 18001 , ISO 9001 and GMP in ( Saudi Arabia , Yaman , Kuwait, Jordon , Sudan , The United Arab Emirates ,Algeria and all over the world.)
Site Master File

About The Company And Activities

Cosmetics Company. Limited is one of the leading manufacturer of Cosmetics in the Middle East located in Egypt S.P.C.C.L. has the following brand on its flag. Id hair care , hydro-best gen-best , sheva and many brands with different shape and pack .

 Objective

  Our aim is that final products must meet the quality standards appropriate to their intended USE to assure consumers health & benefit

Quality System

We have established Quality System Requirements, Our Product contain the correct materials of specified quality & quantity and manufactured under proper conditions accordingly to standard operating procedures.

activities in QC Laboratory

  • TESTING AND APPROVING OF RAW MATERIALS 
  • TESTING AND APPROVING PACKING MATERIALS
  • MICROBIOLOGICAL TESTING FOR BULK/FINISHED GOODS.
  • TESTING AND APPROVING FINISHED PRODUCTS
  • CALIBARTION OF TESTING EQUIPMENTS
  • RETAINING THE RAW MATERIAL, PACKING MATERIAL  AND FINISHED PRODUCT SAMPLES

 

TESTING AND APPROVING THE PACKING MATERIALS

  • PACKING MATERIAL SPECIFICATIONS
  • PACKING MATERIAL TESTING

TESTING AND APPROVING THE RAW MATERIALS

QC chemist draws the samples with for   N+ 1 or  Min 5 nos. of  raw material container  as per the sampling plan given by the QC chemist, chemist  is responsible for testing the raw materials  as per for the specifications and assessment by comparing with the standard sample. QC Chemist enters details of sample in Sample Entry Register,   tests are carried out by QC Chemist as per the test methods given in the SOP’s. Test certificates from vendors are verified for conformance with  the specifica­tions. In case of deviation , the vendor is advised for necessary corrective action. Raw material analysis  are recorded in work book and  reported in the form of Raw Material Report.

All Raw materials from all the other supplier’s are tested on 1: 1 basis. Based on the production requirements only quality cleared Raw Materials are transferred to the manufacturing floor under  “Approved ‘’Status“.

  MICROBIOLOGICAL TESTING

Microbiological tests are carried out as per procedure given in the Microbiological Methods SOP’S.

Microbiological laboratory  need to be maintained for hygiene and other requirements. All analysis need is carried in the ‘Aseptic Zone’

FINAL INSPECTION AND TESTING

The QC inspector checks the product samples as per the Standard Operating Procedures, He records the hourly findings.  checking are also carried out on the finished goods by another QC inspector and findings are reported in the form of Packed product inspection Report . The QC Chemist  gives final clearance for despatches.

CALIBRATION OF TEST EQUIPMENTS

QC Chemist is responsible to maintain a master list of equipment that affect quality.  The list has category wise, the equipment that are to be controlled, calibrated  and maintained. This list also has the Name of the Equipment, Identification No., Location, Frequency of Calibration, Least Count of Equipment,Acceptance Criteria, and whether the equipment is calibrated in house or externally.All Master equipment s and traceability certificates are preserved in the QC laboratory

STANDARDISATION OF REAGENTS           

All reagents used for analysis of raw material and finished products need to be standardises regularly and records are maintained .

SAMPLES AND THEIR RECORDS   

The counter batch samples of finished products are  stored  in stability room . These are analysed Personal Hygiene

  • Protective clothing - clean & hygienic conditions followed
  • Appropriate hand wash facility at the plant entry fixed
  • Washing / disinfecting hands before entry to the plant followed
  • Antibacterial soap / disinfectant solution used for hands cleaning
  • Cutting of Nails – regularly monitored by production supervisor
  • No smoking/eating/drinking in the plant strictly followed by personnel working in the production floor.

Storage:

Storekeeper is responsible for storing of raw material / Finished Product. Storage of raw materials,   stored as per instruction of the manufacturer. Raw materials of different type of specifications will be kept in the racks according to the size and type.

Packaging

Finished product packed as per nature of product. Packing will be carried out by packaging experts to protect our product during handling, transporting, and storage until the customer finally received it.

The packaging material  paper, corrugated paper, etc. will be used to keep gap between one items to other and to prevent them from scratch or chipping.

 

 

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