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Bioequivalence/ Bioavailability Studies

In order to conduct invitro bio-equivalence studies to assure high level of confidence and meet with time-lines the R&D strives to ensure high quality clinical, bio-analytical, statistical and pharmacokinetic data necessary to create international harmonization in bioequivalence testing. The harmonization in the requirements and standards for bioequivalence testing would be achieved by conducting all the studies as per the GCP and GLP regulations and other regulatory guidelines. Different studies have been conducted by nationally recognized and international institutions augmenting the credibility of Efroze products these are as under. Our dedicated research group comprises highly motivated Pharmacists, Chemists, Microbiologists and Statisticians having zeal of creativity and possesses expertise in Development of Research Methodology, Statistical model applications, interpretations, protocol development and validations.



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