Previous Page  7 / 9 Next Page
Information
Show Menu
Previous Page 7 / 9 Next Page
Page Background

allied

academies

Page 32

Journal of Biotechnology and Phytochemistry

Volume 1 Issue 3

Chemistry World 2017

November 13-15, 2017 Athens, Greece

7

th

World Congress on

Chemistry

Bilge Sener, J Biotech and Phyto 2017

Quality control and regulatory issues of

phytomedicines for global health care

H

erbal medicinal products have been playing an

important role in the primary health care of the

people around the world, specially in the developing

countries. In order to treat health problems with the

modern medicines, the production of safe and effective

herbal medicinal products in a standardized way is

essential. Assessment of the quality, safety and efficacy

of herbal medicinal products are an important issue.

Standardization of raw materials, intermediates and

final product of herbal medicines are the main issue for

the quality control of herbal medicinal products. All of the

supporting evidence behind the use of phytomedicines

has been on use of standardized extracts of the plant

material to ensure reproducibility in the clinical setting.

With the growing interest for alternative approaches in

treating diseases, herbal medicinal products have also

an important role for the development of new therapeutic

agents. For this issue, researches should focus on: 1.

characterization of phytomedicines in terms of chemical

composition and biofunctional activity. 2. studying the

effects of certain processing and extraction methods

and parameters on the chemical characteristics of

phytomedicines source materials. 3. development of

chemo-based and bio-based standardization methods

for phytomedicines. Herbal medicinal products named

as “Phytomedicines” exhibit a variety of biological

activities on human health. These range from the

control of regulatory processes by Health Authorities

is essential for human life. Therefore, herbal medicinal

products are also subject to the same legislative

controls as other medicines. The overview of the

herbal medicinal products worldwide along with current

registration guidelines and criteria for the control and

market situation of herbal medicinal products in Turkey

will be highlighted.

Biography

Bilge Sener graduated from Ankara University, Faculty of Pharmacy in 1974.

She has completed her PhD awarded by the Turkish Scientific and Technological

Research Council (TUBITAK) at the Department of Pharmacognosy in 1977. In

1981, she became an Associate Professor. She was involved within the process of

establishing Department of Pharmacognosy, Faculty of Pharmacy, Gazi University

in 1982. She became a Full Professor in 1988. She achieved some researches at

the Department of Chemistry, The Pennsylvania State University (USA) between

1986 and 1988 as Visiting Scientist awarded by National Science Foundation. She

was also involved in several administrative works at Gazi University; as Director at

the Department of Pharmacognosy, Faculty of Pharmacy, Gazi University between

1982 and 2002, as Chair at Division of the Professional Sciences of Pharmacy,

as Co-Director at the Institute of Health Sciences (1988-1994) and as Dean at the

Faculty of Pharmacy, Gazi University (1994-1997). She was given the degree of

Adjunct Professor by University of Karachi, Pakistan. She worked as Director in

48 projects supported by NATO, NSF, IUPAC, Soctrates-Grundtvig, TUBITAK and

Universirty Research Funds by now. She has authored or co-authored 7 books,

85 chapters and 658 research articles published in leading international journals.

She has also given 68 conferences and 313 plenary and invited lectures at the

international symposia in the field of natural product chemistry. She has supervised

5 PhD, 12 MSc at Gazi University as well as co-supervised 17 PhD thesis at the

University of Karachi. She is amember for 14 international and national professional

societies.

bilgesener11@gmail.com

Bilge Sener

Gazi University, Turkey