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Genuine Research Center

Clinical Trial (Phase II IV). GRC is the first GLP based ISO/IEC 17025:2005 accredited laboratory in Egypt. State of Art Laboratory Equipment. Biowaiver and In-Vitro Dissolution studies. GCP compliant clinical facility. In-vitro testing: accelerated stability studies, biowaiver. Bioavailability and Bioequivalence studies. Professional and excellent services with superior and timely performance. Biowaivers and comparative in-vitro dissolution. Development and analytical method validation.

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Genuine Research Center | grc-me.com Reviews

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Clinical Trial (Phase II IV). GRC is the first GLP based ISO/IEC 17025:2005 accredited laboratory in Egypt. State of Art Laboratory Equipment. Biowaiver and In-Vitro Dissolution studies. GCP compliant clinical facility. In-vitro testing: accelerated stability studies, biowaiver. Bioavailability and Bioequivalence studies. Professional and excellent services with superior and timely performance. Biowaivers and comparative in-vitro dissolution. Development and analytical method validation.

<META> KEYWORDS

1 study request

2 useful links

3 about grc

4 accreditation

5 clients and sponsors

6 available assays

7 electronic consent

8 career opportunities

9 bioequivalence studies

10 accelerated stability studies

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study request,useful links,about grc,accreditation,clients and sponsors,available assays,electronic consent,career opportunities,bioequivalence studies,accelerated stability studies,in vitro dissolution studies,welcome,grc profile,excutive team,vacancies

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Genuine Research Center | grc-me.com Reviews

https://grc-me.com

Clinical Trial (Phase II IV). GRC is the first GLP based ISO/IEC 17025:2005 accredited laboratory in Egypt. State of Art Laboratory Equipment. Biowaiver and In-Vitro Dissolution studies. GCP compliant clinical facility. In-vitro testing: accelerated stability studies, biowaiver. Bioavailability and Bioequivalence studies. Professional and excellent services with superior and timely performance. Biowaivers and comparative in-vitro dissolution. Development and analytical method validation.

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grc-me.com

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Genuine Research Center - Available Assays

http://www.grc-me.com/assays.html

Clinical Trial (Phase II IV). Betahistine dihydrchlorid (2-Pyridyl acetic acid metabolite). Biowaivers and comparative in-vitro dissolution. Development and analytical method validation. Solid container 6 months at 40 C/75% R.H. Semipermeable containers for 6 months at 40 C/75%R.H.

2

Genuine Research Center - Clinical Services

http://www.grc-me.com/clinical_services.html

Clinical Trial (Phase II IV). GRC has a dedicated clinical unit for on-site accommodation or to provide ready access to local hospital facilities. Each study is conducted under strict adherence to ICH and FDA GCPs, dedicated to a high level of protocol compliance. All subject-screening activities are conducted in a separate screening area. Biowaivers and comparative in-vitro dissolution. Development and analytical method validation. Solid container 6 months at 40 C/75% R.H.

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Genuine Research Center

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Clinical Trial (Phase II IV). GRC is the first GLP based ISO/IEC 17025:2005 accredited laboratory in Egypt. State of Art Laboratory Equipment. Biowaiver and In-Vitro Dissolution studies. GCP compliant clinical facility. In-vitro testing: accelerated stability studies, biowaiver. Bioavailability and Bioequivalence studies. Professional and excellent services with superior and timely performance. Biowaivers and comparative in-vitro dissolution. Development and analytical method validation.

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Genuine Research Center - Data Management

http://www.grc-me.com/data_management.html

Clinical Trial (Phase II IV). Provides comprehensive support for all phases of clinical trials through:. KineticaTM release 4.4.1. GRC offers comprehensive Data Management capabilities to handle all clinical data generated from a trial. GRC has the expertise and capabilities to fulfill your specific data management requirements and provide clarity to your study data. CRF Design (including completion guidelines), annotation, printing. Handling of CRFs and Data Clarification Forms (DCF).

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Genuine Research Center - Study Request

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Clinical Trial (Phase II IV). Test Product’s Dosage Form:. SPONSOR'S / TEST PRODUCT MANUFACTURER. Reference Product’s Dosage Form:. Required to be filled by customer. Biowaivers and comparative in-vitro dissolution. Development and analytical method validation. Solid container 6 months at 40 C/75% R.H. Semipermeable containers for 6 months at 40 C/75%R.H.

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