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| Panacea Biotec Limited |
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Thank you for the good news and the approval document.
I would like to congratulate the team at FCRL for achieving this milestone in the study.
Would like to specially appreciate Dr. Mir who has demonstrated exemplary skills in critical review of the documents and persistent and systematic follow-up with all stakeholders resulting in the EC approval. His foresight and effective risk anticipation and mitigation strategies are really commendable. We are sure of successful completion of this study under the supervision of Dr. Mir and leadership of Dr. Deepak.
Dr. Mudgal Kothekar
Deputy General Manager, Clinical Research
Panacea Biotec Limited
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| AddClin Research |
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We hereby declareth at AddClin Research (Pty) Ltd has been doing business with Fortis Clinical Research Limited, Sunflag Hospital & Research Centre, Faridabad (Haryana), India with great satisfaction. The standard of their work is exceptionally high, as is their scientific inteqrity and quality.
On a personal level, we find them always friendly, approachable and understanding. It must also be mentioned that their turnaround time is fast and their deadlines met, befitting the highly professional company that they are.
Based on first-hand experience, we can honestly recommend them for any project or assignment in our very competitive industry.
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Dr Jacques Malan
Medical Advisor and PrincipaI lnvestigator
AddClin Research (Pty) Ltd. |
Dr Sanet Aspinall
Managing Director
AddClin Research (Pty) Ltd. |
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| RANBAXY |
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We hereby declare that Ranbaxy Research laboratory has been doing business with Fortis Clinical Research Limited (FCRL), Sunflag Hospital and Research Center, Faridabad (Haryana), India since 2008. The Project assigned to them were completed within committed timelines and to our satisfaction.
The facility follows international standards and the team at FCRL has technically sound people to perform the job efficiently.
Based our experience, we believe that the facility has the competence for doing any relevant project or assignment to be submitted to any international regulatory agency across the globe.
Dr. Tausif Monif
Vice President
Clinical Pharmacology & Pharmacokinetics
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