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Bioequivalence Studies

Offering you a complete choice of services which include Clinical Research, Turn-key pharma projects, BA/BE Studies (From US FDA Approved CROs) and Expert Reports.

Clinical Research
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Clinical Research

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Afra Pharma consultant offer to conduct, manage and monitor multicentre Clinical Trials in a wide range of therapeutic areas and monitor BE studies in India and abroad. We have a special interest in Independent Clinical Trial Monitoring Work in India and abroad for sponsors from India and abroad.

  • Medical Writing & Clinical Studies
  • Bioavailability
  • Bioequivalence
  • Clinical Trial Studies
  • Analytical Solutions

Reports on

  • Bio availability / Bio equivalence Studies
  • Clinical Trials studies
  • Prepare Periodic Safety Update report (PSUR)
  • Preclinical studies like Toxicity, Carcinogenicity, and Teratology & Reproduction toxicity
BIOSCIENCES SERVICES:

We are in association with ISO certified, ICHGCP compliant Clinical Research & Consulting firm which is dedicated to provide clinical study related services for pharmaceutical and biotechnology product development sculpted to offer high quality design, conduct and analysis of a clinical trial which constantly try to innovate in order to provide easy solutions to our clients for their prestigious projects. To accomplish this, we strive to provide our clients with exceptional services under one roof for the vast sector of Clinical Trial management and Bioinformatics developments.
In Clinical Research, our services range from Site Services to Sponsor related, regulation of Monitoring issues, management of the Clinical Trial data, precise Scientific Writing and the developing Post Marketing Strategies; strictly adhering to the respected regulatory compliance summed up with our personal commitment to time management and unbiased report submissions.
 

ANALYTICAL BIOTECHNOLOGY SOLUTIONS:

Managed by well qualified experienced technicians with immense know how in pharma industry to their credit. With well planned and robust infrastructure, solutions are provided keeping the clients requirement at priority using the latest and high end technologies.
Our team works under close guidance of expert scientists with vast experience in analytical Testing and Pre-clinical studies (LS-MS/MS, HPLC and GC).

  • Analytical Development
  • Analytical Instrumentation
  • Protein Identification and Characterization
  • Pharmacokinetics
  • Nutraceuticals
  • Forensic Analysis
  • Genetic engineering/ Transgenic Technology
  • Agricultural Biotechnology
  • Environmental Biotechnology
  • Industrial Biotechnology
  • Medical Biotechnology
  • Food Biotechnology
  • Cell And Tissue Culture
  • Nanotechnology

Bioinformatics

Bioinformatics uses advances in the area of computer science, information science, and computer and information technology, communication technology to solve complex problems in life sciences and particularly in biotechnology.

Big Data Solutions:

  • Customisation
  • Integration
  • HTS
  • Data Normalization
  • Text Mining Solutions
  • Proteomics

Drug Discovery Solutions:

  • In-Silico Developments
  • Computer Aided Drug Discovery Solutions

 

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Turn-key pharma projects
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Turn-key pharma projects

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Afra Pharma Consultant has collaboration with an ISO 90001 certified worldwide

Pharma consulting and engineering company with more than 1600 people at more than 20 locations worldwide and handles up-gradation projects to turn key projects in

Pharmaceuticals, Biopharmaceuticals, Medical devices, vaccines and industrial biotech and API.

 

 

We offer professional services to clients’ specific requirements and take pride in providing current top quality STATE OF THE ART ENGINEERING.

We undertake comprehensive management of all project activities, right from conception through completion of construction and commissioning, including Continuous Monitoring, thereafter to achieve the projected savings in time and money to add value to our services for the benefit of our clients.

We also assist in the up gradation of plants in accordance with the latest industry standards.

We are proud to state that the Facilities we have successfully commissioned, in India and Abroad, have complied with the demanding standards and requirements of International companies like conforming to cGMP requirements and US FDA & UK MCA guidelines.

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BA/BE Studies (From US FDA Approved CROs)
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Afra Pharma consultant offer to conduct, manage and monitor multicentre Clinical Trials in a wide range of therapeutic areas and monitor BE studies in India. We have a special interest in Independent Clinical Trial Monitoring Work in India and abroad for sponsors from India and abroad.

  • Medical writing
  • Bioavailability and Bioequivalence
  • Clinical trial studies
  • Analytical solutions

Reports on:

  • Bioavailability and Bioequivalence studies
  • Clinical trial studies
  • Prepare Periodic Safety update report (PSUR)
  • Preclinical studies like toxicity, carcinogenicity, Teratology and Reproduction toxicity

View Complete Details

Yes, I am interested!

Expert Reports

Expert Reports

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