About US About OctoberPharma
About October Pharma
October Pharma (OP) S.A.E is an Egyptian enterprise molded by global aspirations. This has always demanded a preparedness and long- term organizational vision that can encompass the turbulence's and paradoxes of shifting terms and terrain's of business. October Pharma (OP) is producing different pharmaceutical dosage forms of products under cGMP rules & regulations:
Solid (tablets, capsules & powder)
Liquid (syrup, drops, solution & spay)
Soft Gelatin Capsules
Ampoule & Vial
Cream & Suppository
Powder
# Quality, Environmental and Occupational Health And Safety Policy .pdf
Quality Management System
The quality Assurance has a great role in the development and maintenance of the company’s quality system. This is achieved by a combination of systematic sampling, testing validating, monitoring and auditing of materials, facilities, systems and procedures which can influence the quality of our products. Authorized and approved standard operating procedures for all operations are used.
This includes production, quality control, quality assurance, materials management, warehousing, distributing, Information Technology, safety controls, housekeeping, sanitation, and engineering. Quality assurance has to ensure that these procedures are adhered and records are maintained.
Any deviation is investigated and documented. Corrective action is taken wherever necessary. Periodic self inspection and auditing are conducted to monitor the effective implementation of the current good manufacturing practice and quality system.
Suppliers of key starting materials and analytical laboratory reagents are chosen according to high quality parameters and are assessed according to validated and standardized procedures.
Records generated via the implementation of the quality system are controlled and maintained according to authorized and approved procedure.
Management review for the quality system is carried out periodically.
Each product is subjected to appropriate types of testing and control according to the specifications approved by the regulatory authorities and the redefined quality parameters. Records generated from the whole processes concerned with the production of the product are well revised and checked before the release of the product. Stability evaluation according to pre-defined protocol.