Curriculum Vitae
Dr. Heba Mohamed Elbedaiwy
Associate Professor of Pharmaceutics
Faculty of Pharmacy – Damanhour University
Personal:
Name
:
Heba Mohamed Mokhtar ElBedaiwy
Current title
Address
5Abdelsattar Mansour Street, Louran , Alexandria , Egypt.
Telephone
Mobile: +2 01227440813, 01154620826
Home: +2 035840137
e-mail
hebaelbedaiwy@yahoo.com.
Heba.elbedaiwy@pharm.dmu.edu.eg
Date of Birth
August 5th 1977
Place of Birth
Tanta, Egypt
Religion
Muslim
Nationality
Egyptian
Marital Status
Married
Qualification degrees:
Title thesis: "Studies to enhance the intestinal absorption and bioavailablity of acyclovir"
Title thesis: "A study to investigate the effect of liquisolid technique on the dissoliution characteristics of a model class II drug"
PositionOccupied
2022 to present
2012-2022:
Associate professor of Pharmaceutics, Faculty of pharmacy, Damanhour University, Damanhour, Egypt.
Lecturer of Pharmaceutics, Faculty of pharmacy, Damanhour University, Damanhour, Egypt.
1999-2006
Research pharmacist at the Bioavailability Unit at PSC, Faculty of pharmacy, Tanta University, Egypt.
Brief description of duties:
Teaching Courses in Faculty of Pharmacy, Damanhour University, Damanhour, Egypt:
Workshops and Courses:
Courses and workshops held in the Faculty and Leadership Development Project (FLDP), Egypt:
Academic activities:
Community Involvement / Administrative Activity:
Practical and Research Experience
Human studies:
Animal studies:
Analytical techniques:
HPLC (UV& Fluorescence) and UV spectroscopy.
Computer packages:
Pharmacokinetic data analysis with WinNonlin.
Statistical packages such as Minitab and SPSS.
Publications:
SA Helmy, Heba M El-Bedaiwy. Comparative in vitro dissolution and in vivo bioavailability of diflunisal/naproxen fixed-dose combination tablets and concomitant administration of diflunisal and naproxen in healthyadult subjects. Drug research 34 (03), 150-158
SA Helmy, Heba M El-Bedaiwy, SM El-Masry. Applying Biopharmaceutical Classification System criteria to predict the potential effect of Cremophor® RH 40 on fexofenadine bioavailability at higher doses. Therapeutic Delivery 11 (7), 447-464