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12 May

HARVEST 14 Exhibition: Celebrating Creativity, Innovation, and Sustainable Design

The Faculty of Arts and Design at October University for Modern Sciences and Arts (MSA University) is pleased to announce the upcoming HARVEST 14 Exhibition, a flagship annual event celebrating student creativity, innovation, and sustainability. Building...

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Bioanalytical Part

Facilities:ย 

  • LC-MC/MS systems. {(UP) LC-MS โ€“ Waters}

  • HPLC System:

    • Agilent

  • ย Microbalance.

  • All study samples are stored in controlled freezers (-20ยฐC and -70ยฐC).

  • UPS (Uninterrupted Power Supply) and generator back-up.

  • Services

    • Method Development.

    • Method Validation.

    • Bio-Waiver / Bioequivalence.

Data Management Part

  • Non-compartmental pharmacokinetic analysis using Winnonlin software.
  • Assessments of Bioequivalence.
  • Tabulation, graphical display, analysis and interpretation of study data.
  • Study design and development of Protocol and Informed Consent Form (ICF).
  • Designing of Case Report Form (CRF) as per protocol requirements.
  • Preparation of Bioequivalence Report, Clinical Report, Analytical Report and Statistical Report.
  • Sample Size Estimation and Randomization.

Clinical Part

  • Screening area for physical examination.
  • Sample collection rooms.
  • Complete examination of volunteers with close monitoring during two study phase for the expected AE/SE.
  • Notify the drop-out volunteers with a copy from his analysis report, and follow them up.
  • The BE Center contracted with neuroespitalia hospital.
  • First Aid cupboard.
  • Dining room.
  • Storage freezers ( -80 and -20ยบ C).
  • Archives for secure document storage.

Quality Assurance System

Quality Assurance Unit ensures that studies are performed in accordance with Good Laboratory Practice (GLP)-Good Clinical Practices (GCP) regulations and through in house procedures.
Also, it is responsible for document controlling of study protocols, analysis plans, SOPs & policies; and ensuring the updated versions of these controlled documents are effective and in place or accessible to relevant staff.

QA unit is responsible for regular auditng which include:

  • Study source documentation, procedures, and reports; and provides regulatory advice and support to the operational staff.
  • Facility & system, to check adequacy & eligibility of resources and proper utilization of provisions.

Bioequivalence Center - Contacts

  • 26 July Mehwar Road intersection with Wahat Road, 6th October City. Egypt.
  • Tel. : (+202) 38371534-5-7/ Ext: 5146
  • becenter@msa.edu.eg
  • Hotline : 16672
  • Center Manager: Dr. Dina Karam +0201129801960
  • QA Manager: Dr. Aya Badr +0201112006907

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