This is the Prime and the MOST FOCUSED area and field of the company. GMD has taken great care to ensure that there are no pages left unturned when it comes to quality control. The company is committed to deliver product of the Highest International Quality, comparable to the best in the world to its partners and associates. From raw material purchase till dispatch the company ensures that all necessary care and procedures are followed and also validated simultaneously to make sure that quality is not compromised anywhere and also Quality Standard Procedure is maintained.
Raw materials are sourced from various parts of the world and are procured from the best, reliable and quality international manufacturers. One of the standard procedures of the company while procuring the raw material is the periodical visits to the manufacturing facilities of these suppliers to ensure that the raw material we purchase are produced/procured from a quality establishment and all necessary quality control measures are adhered to so that quality raw material reaches us.
On its part the company has a very strict norm and procedure in respect to quality control. From receipt to packaging the company has laid strict guidelines which are being followed devotedly by each and every member. Certain features which the company has in terms of Q & A are:-
* Entire manufacturing facility is under the CLEAN ROOM concept, with clean room of class 10000.
* The Air Handling Unit (AHU) in the clean room filters air upto 0.3 Microns using Pre, Fine and HEPA filters. The products are manufactured in compliance and as per the norms of Good Manufacturing Process (GMP)
* All entry and Exit points of manufacturing areas are provided with Air Showers or Air Curtains.
* The company is in the process of getting ISO 9001, CE and GMP certifications. Mid term plans include getting certification from US- FDA, Since the company manufactures 2 part Syringe, each and every syringe is checked for le
Team / Manpower
The company is promoted and managed by:-
Mr. A. R. Shaikh
The Founder and Chairman of the company, he envisioned and successfully took up the challenge of setting up a world-class medicare unit. A 30 years veteran in the health and health related industry, it was under his expert supervision and guidance that the manufacturing unit was conceived, planned and built.
Aim / Vision / Mission
Goa Medicare Devices has a vision of being a global leader in the field of manufacturing medical disposables. Already the third largest syringe exporter in india, it aims to be the single largest exporter of india by 2010.
Infrastructure
A 100% Export Oriented Unit (EOU), Goa Medicare Devices is registered with the Ministry of Commerce, Government of India. The advanced manufacturing facility is built to confirm to stringent international standards with state of the art technology from Japan and Germany. Designed in accordance with the guidelines of GOOD MANUFACTURING PRACTISE (GMP) for sterile medical devices, we ensure consistent and superior quality every time.
Our Facilities
A 100% Export Oriented Unit (EOU), Goa Medicare Devices is registered with the Ministry of Commerce, Government of India. The advanced manufacturing facility is built to confirm to stringent international standards with state of the art technology from Japan and Germany. Designed in accordance with the guidelines of GOOD MANUFACTURING PRACTISE (GMP) for sterile medical devices, we ensure consistent and superior quality every time.
Our Manufacturing Unit
Goa Medicare Devices has a well planned manufacturing facility, the manufacturing area, which is a CLEAN ROOM, is completely air conditioned, with AIR HANDLING UNIT (AHU) of class 10000 . The entire manufacturing area is well monitored and the air in the manufacturing plant is filtered up to 0.3 MICRONS. From the Electrical such as Clean Room Fittings" to the Vinyl Flooring, every small aspect of the area is well planned and executed. The Sterilization Process which is vital in making the Product Sterile is a special process and is cordoned off from the rest of the area to ensure sterile and non sterile products are kept separately in accordance with the GMP standards. The Sterilization process also complies with the EN 550 norm.
The full fledged in house lab has experienced Q.C. personnel who monitor the manufacturing process round the clock as well as carry out periodic sampling from time to time with full reports and Monitoring Schedule Analysis as per the WHO-GMP guidelines. The Factory laboratory is well equipped to carry out STERILITY, TOXICITY and PYROGEN tests. We have committed by engaging ourselves in creating a safe and reliable product, as this is not just commercial process, but a social commitment to the masses at large, the commitment to produce safe product and economically affordable one too.
About The Founder
The company is promoted and managed by:-
Mr. A. R. Shaikh
The Founder and Chairman of the company, he envisioned and successfully took up the challenge of setting up a world-class medicare unit. A 30 years veteran in the health and health related industry, it was under his expert supervision and guidance that the manufacturing unit was conceived, planned and built.
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