| All our products are manufactured using advanced methods and machinery and, more importantly, through advanced manufacturing processes. A world-renowned leader for process-quality accreditation, DNV of Denmark, has audited our processes. MGRM Group is perhaps the only one in the area of rehabilitation that has its products and processes evaluated by the world quality organizations and obtained all certifications relevant for the industry. |
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| US-FDA & CE (Clinical Approvals) |
MGRM Splints undergo extensive clinical tests.
MGRM has the United States – Food and Drug Administration registration required for marketing products in the United States and the Americas.
MGRM also has the Certificate of Conformity (CE Marking) required for marketing in Europe and other approved countries.
MGRM has cleared toxicological and clinical trials in a variety of countries in Asia, Middle East and other continents.
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| ISO 9001: 2000 / ISO 13485:2003 – Quality Standards |
| ISO 9001 is awarded to MGRM for its "quality management". This certification endorses that MGRM fulfills the following important norms |
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Customer's quality requirements |
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Applicable regulatory requirements, while aiming to |
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Enhance customer satisfaction, and |
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Achieving continual improvement of its performance in pursuit of these objectives. |
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| ISO 13485:2003 is awarded for its specific compliance with respect to MGRM medical devices that meet |
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Customer's quality requirements |
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Applicable regulatory requirements |
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| ISO 14001:2004 - Environmental Management System Standards |
| The ISO 14001 is awarded to MGRM for its "environmental management". This certificate endorses that MGRM: |
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Minimizes harmful effects on the environment and |
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Achieves continual improvement of its environmental performance |
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| OHSAS 18001:1999 - Occupational Health and Safety Management System |
MGRM is awarded OHSAS 18001:1999 indicating that all risks pertaining to occupational health and safety at MGRM Manufacturing sites have been taken care, and have been eliminated or minimized. It indicates that MGRM is also aware of such risks and regularly audits and eliminates them as and when the issues arise.
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| WHO GMP - Good Manufacturing Practices |
World Health Organizations Good Manufacturing Practices (GMP) is a system that ensures that MGRM Products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in production that cannot be eliminated through testing the final product.
The main risks are |
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Unexpected contamination of products, causing damage to health or even death |
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Incorrect labels on containers, which could mean that patients receive the wrong product |
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Insufficient design resulting in ineffective treatment or adverse effects. |
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GMP covers all aspects of MGRM production, from raw materials, premises and equipment to training and personal hygiene of staff. Detailed, written procedures are available for each process that could affect the quality of the finished product.
MGRM system provides documented proof that correct procedures are consistently followed at each step in the manufacturing process - every time a product is made. WHO has established detailed guidelines for good manufacturing practice with which MGRM complies.
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