Tel : (+968) 24502415
 Fax :(+968) 24502297
 Salalah Factory
 Tel :(+968) 23219296
 Fax :(+968)  23219295
 E-mail :
 Website :


Quality is the watchword
At Oman Pharmaceutical Products, all actions are driven by a single-minded commitment to Quality. The principles of Total Quality Management, pervades all departments and is a way of life for our highly motivated workforce.

The fully equipped, sophisticated Quality Control Laboratories, installed with latest computerized analytical instrumentation and equipments, control and test every stage of formulation development and production. These equipments benchmark and test everything from raw materials to packing materials to finished products, besides in-process testing. Special emphasis is laid on Validation, Stability Studies and Bio-clinical studies.

Complementing all the latest instruments and equipments is a dedicated team of highly qualified and experienced scientists. Continuous training and orientation programs ensure that employees are kept abreast with the latest trends and demands of a dynamic Regulatory environment.

Regulatory & Documentation Support
Today’s fiercely competitive and highly regulated markets demand rigorous design and management of product development and registration strategies for success.

Critical time is saved in getting the product to the market in optimum period for submission to the Regulatory Authorities. At Oman Pharmaceutical Products, a team of highly qualified scientists and technical professionals working as part of our Regulatory Affairs, Quality Assurance and Documentation Department help provide important services like: 

  • Domestic and International registrations.

  • Technical bulletins containing Pharmaceutical, Clinical and Therapeutic updates.

  • Site Master file, Abbreviated Application and Dossiers.

  • Liaison with Regulatory authorities for Audits, Inspection and Technical Queries.

Highlights of the OPP Project in Salalah

  • Infrastructure built as per cGMP guidelines and adheres to requirements laid down by MOH, WHO GMP, UK MCA, EU Regulations, US FDA and other international regulatory authorities.

  • The project was implemented by reputed consultants and contractors, selection of machinery was done from highly reputed manufacturers, international consultants advised and evaluated in critical areas of validation, regulatory affairs and marketing.

  • Control And Monitoring Systems (CAMS) installed for the management of HVAC, Fire alarms and Utilities of the total facility.

  • Environment Protection systems like dust collectors, scrubbers, effluent treatment plant, solid waste disposals in place.

  • Well-trained and experienced staff appointed for formulation development, production, Quality assurance, Quality control and training departments apart from engineering and administration.

  • Segregated and dedicated areas for products containing Antibiotics, Hormones and Steroids.

  • Production Capacity

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