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Providing bio equivalence study services.+ Read More

Nature of Business

Service Provider

Total Number of Employees

26 to 50 People

Year of Establishment

2004

Legal Status of Firm

Limited Company (Ltd./Pvt.Ltd.)

Annual Turnover

Upto Rs. 50 Lakh

GST Number

06AAACO7343M1Z7

Bio Equivalence Study
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Bio Equivalence Study

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Choosing an appropriate partner for your drug development process is the most critical step in Clinical Research. FCRL provide innovative, effective and most comprehensive research services for your Clinical Trails needs through its association with highly experienced Investigators belonging to Fortis Hospital network.

FCRL provides full range of services for Phase I in healthy volunteers (NMEs and generic products), Phase I in oncology, Phase II – IV in patients as well as bioequivalence studies in healthy volunteers and patients.

Full Spectrum of  Services are provided by FCRL under one roof :

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Bio Equivalence Study Services
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A well established IT infrastructure is at the core to provide valued driven research at Fortis Clinical Research.The IT infrastructure at FCRL includes the following state of the art hardware & software technologies:


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Bioavailability Studies

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Our project managers are medically qualified doctors with vast experience in end to end management of clinical trials. Project managers are a key for the successful completion of any clinical trial. Our project managers bring with them therapeutic expertise and experience of working on global clinical trials; having successfully cleared various sponsor audits and inspections.

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Bioequivalence Studies

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Fortis Clinical Research has a team of medical writers with extensive medical writing knowledge, writing skills and vast experience in Pharma & Biotech companies and CROs.

The team excels in providing quality data with quick turn around time. the Medical writing services includes:

Regulatory Writing

Clinical Trial protocols (ICH E6)

Clinical study reports (ICH E3)

New drug applications (NDA)

Abbreviated New drug applications (ANDA)

Clinical sections of common technical document (CTD and eCTD)

Periodic and annual safety update reports

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