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I 3 Consulting Offers Reliable Medical Device Consultancy At Competitive Prices

Several industries such as food, drugs and cosmetics come under strict regulatory practices. Entrepreneurs need to learn about all these regulatory principles to take correct and timely decisions to ensure the sustainable development of their businesses. Operating from India, I 3 Consulting offers an incredible range of consultancy services for new as well as established businesses and guides its clients to put the right foot forward. Even though the company operates from India, it serves global clientele that is growing day-by-day. The company has a team of experienced and qualified professionals from various backgrounds, such as medical devices, pharmaceuticals, cosmetics, food and nutraceutical regulatory practices, which offers their expertise to provide solutions for different regulatory challenges faced by clients.

Responding to queries regarding the consultancy services on offer, one of the senior executives working with I 3 Consulting in a recent interview stated, “We are regulatory specialists committed to help clients, so that they can take the right decision and follow the relevant regulatory practices closely. We have experience of working with clients spread across America, Europe, Middle East and Asia Pacific. We are capable of offering comprehensive services to firms with a focus on the development of drug master files with the United States Food & Drug Administration or FDA. Our annual DMF maintenance services include responding to FDA concerns about USDMF submitted by client, notifying about any changes in the submitted US, FDA, DMF and providing DMF changes, additions and deletions to the FDA that give our clients an edge over their competitors.”

I 3 Consulting enables medical device component manufacturers, finished good manufacturers, medical software developers, medical device designers and developers and pharmaceutical suppliers procure ISO 13485:2012 certification. It helps them prove that they manufacture products or devices in a safe and effective environment or facility. I 3 Consulting provides the necessary training, documentation, implementation and internal audit to help clients make their organization eligible for ISO 13485:2012 certification.

“We are medical device consultants with good knowledge and exposure to the US FDA regulations in all the classes of devices. Marketing medical devices in Europe is allowed only after affixing CE mark, while it is possible after establishment registration and product listing in the US. Our unique, comprehensive approach helps us offer a wide range of services designed to enable clients export medical devices to the USA and Europe quickly and safely,” further added the senior executive.

I 3 Consulting helps OTC drugs, drug testing laboratories, dietary supplements, homeopathic drugs and active pharmaceutical ingredient or API manufacturers sell their products in the US market by completing their FDI registration. It also helps organizations to comply with 21 CFR Part 820 of the US Federal Law and complete 510(k) applications quickly and successfully. For those who are looking for medical device consultants, I 3 Consulting can be the right company to deal with.

About I 3 Consulting:

I 3 Consulting is the leading consultation service provider based in India that caters to the regulation compliance requirements of a global clientele. With offices in the US, the company offers comprehensive consultation to a large number of clients. I 3 Consulting is large enough to assist Fortune 500 companies and small enough to guide individually owned companies, which make it one of the most trustworthy organizations for FDA Drug Master Files consultation.  

Contact Information

  • Name: i3c Global Consulting

    Company: i3c Global Consulting

    Telphone: -- , -

    Address: I 3 Consulting
    BANGALORE – 560029
    FAX + 91 804 160 8963
    FAX + 1 815 986 2632