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Student Program
Safety and Risk Management Conference
  • Career Opportunity Presentation

  • Paper Presentation Competition

  • Poster Display Competition

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2016 2015
2014  
Contact : Mr. D. L. Pandya
Classic Computer Services
B-4, Mandir Appt., Opp. P & T Colony, Jodhpur Char Rasta, Satellite Road, Ahmedabad-380 015. India.
Phone : +91 79 26740611 Telefax : +91 79 26754867
M : +91 9825457563
E-mail : mpds00@vsnl.com / dlpandya@gmail.com

SYMBIORPH CLINICAL TRIALOGY

Medical Device Regulatory Compliance Consulting Company

 

Symbiorph Clinical Trialogy is Ahmedabad based medical device regulatory compliance advising company.

 

We support the medical device manufacturer to realize the concept of “MAKE IN INDIA” and help them in Global Medical Device Product Registration.

 

Core Services

 

  • Indian Medical Device Manufacturing License as per revised requirements

  • CE Marking

  • US FDA 510K

  • Risk Management-ISO 14971

  • Clinical Evaluation-MEDDEV 2.7.1 Rev 4, June 2016

  • Medical Device Software Validation (IEC 62304)

  • Usability Engineering (EN 62366)

  • IEC 60601-Compliance

  • Sterilization-EO Validation (ISO 11135)

 

Global Product Registration

 

  • US FDA 510K,

  • Latin America (Brazil, Mexico etc.);

  • South East Asian (Thailand, Australia etc.);

  • MENA (Egypt, Israel etc.);

  • GCC (UAE, Saudi, Kuwait etc.)

  • CIS (Russia, Kazakhstan etc.)

We are advising the medical device manufacturers in such a manner that they can appoint more than ONE distributors in these countries, thereby to remove the dependency on the single distributor.

 

Contact Details:
Siddharth Jain, Chief Regulatory Advisor
Mobile:+91-9998038576
E-mail: siddharth@symbiorph.in;
Website:www.symbiorphclinicaltrialogy.com
Address: 1365, Jalkukadi Ni Pole, Behind Raipur Post Office, M.G Haveli Road, Manekchowk, Ahmedabad-380001, Gujarat, India