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Hospitals & Health care

GMP - Good Manufacturing Practice

Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.

GMP covers all aspects of production from the raw materials, premises, and equipment to the training and personal hygiene of staff. GMP ensures procedures are followed at each step of manufacturing. GMP refers to the Good Manufacturing Practice regulations promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug, and Cosmetic Act. These regulations, which have the force of law, require that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective.

ISO 13485:2016 - Medical Devices - Quality Management Systems

A medical device is a product, such as an instrument, machine, implant or in vitro reagent, that is intended for use in the diagnosis, prevention and treatment of diseases or other medical conditions.

ISO 13485 is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services. It can also be used by internal and external parties, such as certification bodies, to help them with their auditing processes.

Organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities (e.g. technical support).

ISO 13485:2016 can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations.

Benefits of ISO 13485:2016 Certification

Improved credibility and image
Improve customer satisfaction


Continual improvement
Improve processes and decision making


Better employee engagement

ISO 29990:2010 - Learning Services


ISO 29990:2010 specifies basic requirements for providers of learning services in non-formal education and training.

The objective of ISO 29990:2010 is to provide a generic model for quality professional practice and performance, and a common reference for learning service providers (LSPs) and their clients in the design, development and delivery of non-formal education, training and development. ISO 29990:2010 uses the term “learning services” rather than “training” in order to encourage a focus on the learner and the results of the process, and to emphasize the full range of options available for delivering learning services. Organizations will be offered more flexibility with standards dealing with learning services on one hand and standards addressing management systems on the other hand. This new standard offering will give educational and training providers new possibilities and opportunities.

NABH - National Accreditation Board for Hospitals & Healthcare Providers

NABH (National Accreditation Board for Hospitals & Healthcare Providers) is a constituent board of Quality Council of India, set up to establish and operate accreditation programme for healthcare organizations.

It is a body which operates accreditation and allied programs on patient safety and healthcare quality. The standards, evaluation and certifications are based upon national/international norms, through a process of self and external evaluations. NABH accreditation applies to Hospitals, Ayurveda centres, Wellness centres, blood banks, dental facilities etc. Accreditation to a health care organisation stimulates continuous improvement. It enables the organisation in demonstrating commitment to quality care. It raises community confidence in the services provided by the health care organisation. It also provides opportunity to healthcare unit to benchmark with the best.

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