دکتر اصغریان گروه

تعداد بازدید:۷۲

 

Curriculum Vitae

Ramin Asgharian

PROFILE

Sex: Male

Nationality: Iranian

Country of residence: Iran

Current position: Member of Faculty

University: Islamic Azad University (IAU)

Email Address: ramin3205@gmail.com

WORK EXPERIENCE

Mar 2008 – Present: Faculty of Pharmacy Islamic Azad University Tehran, Iran Member of Faculty in Pharmaceutics Department.

Teaching courses on:

  • Physicochemical Control (Theoretical and practical)
  • Microbial Control (Theoretical and practical)
  • Pharmaceutics (Theoretical)
  • Industrial Training
  • Analysis and Control
  • The Laws Governing of Pharmaceutical Affairs
  • GMP

Manager Department of Basic Sciences for one year

Manager Deartment of Pharmaceutics for 2 years

Educational Assistant from 2016 until now

Being Guide and Consultant of several theses in pharmaceutical, managing and marketing.

Mar 2008 – Present: QA (Quality Assurance) Consultant of some Pharmaceutical Company (Cobeldarou, Abidi)

Sep 1998 – Sep 2008: Jaber-Ebneh-Hayyan Pharmaceutical Company Tehran, Iran

Last Position: GMP Manager & Regulatory Deputy

This company was active in production and sales pharmaceutical finish products, particularly antibiotics.

I was responsible for:

• Establishing GMP regulatory.

• Managing to prepare Standard Operation Procedures (SOPs).

• Confirming the GMP checklists.

• Inspecting other companies who produce API for Jaber-Ebneh-Hayyan Company.

  Previously I have worked as a R&D Expert for two years and before that I had worked as chief of microbiology laboratory for four years.

My main achievements in this job include:

• Inspection of some International pharmaceutical companies.

• Establishing the internal GMP audit.

• Formulation of some pharmaceutical products.

• Establishing method validation of some of the microbial tests.

May 1997 - Sep 1998: Sina Darou Pharmaceutical Company, Tehran, Iran

Position: R&D Expert

The company was active in production and sales pharmaceutical finished products particularly ophthalmic drugs.

I was responsible for:

• Formulation and control of new finish products.

• Improving old formulations.

Main achievements:

• I have formulated some products such as Cromolyn ophthalmic drops, Cromolyn nasal

Spray, Flourometolne ophthalmic drops.

May 1996 - May 1997: Pasteur Institute Tehran, Iran

Position: chief of laboratory

I was responsible for:

• Managing all of laboratory tasks.

• Managing to prepare Standard Operation Procedures (SOPs).

Sep 1995 - May 1996: Kosar Pharmaceutical Company Tehran, Iran

Position: laboratory Expert

The company was active in production and sales pharmaceutical finish products, particularly antibiotics.

I was responsible for:

•Working with many analytical instruments such as HPLC, GC, Potentiometer, and …

EDUCATION

Oct 2000 - Sep 2006: TehranUniversity, Pharmaceutics, Doctorate (PhD), Tehran,

Iran

Feb 1988 - May 1996: AzadUniversity, Pharm D, Doctorate, Tehran, Iran

CERTIFICATES

  1. Participated in the International Workshop of GMP and GLP Practices in Health Related Industries which was held at Pasture Institute of Iran 2-4 March 2013.
  2. Certificate Of Completion For Industrial Microbiological Training By Sanofi Aventis.
  3. Certificate Of Completion For Taxoter Monovial Technology Transfer By Sanofi Aventis.
  4. Certificate Of Completion Course in “Pharmaceutical Marketing Workshop” (20th Agu. To 16th Oct.2009)
  5. ISO 14001:2004 & OHSAS 18001:1999
  6. TQM odel, Iran ISO-9000 Internal auditor training course SGS , Iran
  7. Freeze Drying Process ICI Industry S.P.A , Italy

PUBLICATIONS and SEMINARS

  1. Z. Vatanparast, R. Asgharian, S. A. Mortazavi and K. Gilani. Efficiency improvement of fluticasone propionate dry powder formulation for inhalation in pulmonary patients. Medical Science Journal of Islamic Azad University, Tehran Medical Branch (2016), 26(1): 1-5.
  2. P. Rostami, R. Asgharian, A. Abdollahpour and F. Mahdavizadeh.  Cleaning Validation for Residual Estimation of Ceftizoxime on Surface of Pharmaceutical Manufacturing Equipments.  International Journal of Review in Life Sciences. Volume 6 (2016), Issue 1 (Jan-Mar), Pages 16-27
  3. A. Merrikhi Khosroshahi, F. Aflaki, N. Saemiyan, A. Abdollahpour, R. Asgharian. Simultaneous determination of paracetamol, 4-Aminophenol, 4-Chloroacetanilid Benzyl alcohol, Benzaldehyde and EDTA by HPLC method in paracetamol injection ampoule. Journal of Pharmaceutical and Health Sciences 2016;4(1), 61-69.
  4. E. Oveili, R. Asgharian, A. Abdollahpour. Determination of Residual Ceftazidime in Pharmaceutical Product line: A Cleaning Validation Study by HPLC. Journal of Pharmaceutical and Health Sciences 2016;4(1), 53-59.
  5. F. Shokraneh, R. Asgharian, A. Abdollahpour, M. Raminb, A. Montaseri and A. Mahboubi.  A Novel High Performance Liquid Chromatographic Method for Determination of Nystatin in Pharmaceutical Formulations by Box– Behnken Statistical Experiment Design. Iranian Journal of Pharmaceutical Research (2015),14 (Supplement): 43-49
  6. R. Asgharian, F. Mehtarpour, A. Heydari. Step by Step How to Do Cleaning Validation. International Journal of  Pharmacy & Life Sciences. 3345-3366, March, 2014.
  7. Z. Vatanparast, R. Asgharian, Z. Daman, K. Gilani, S. A. Mortazavi. Evaluation of the combined effect of cyclodextrin and lactose on aerosolization capability of fluticasone propionate microparticles. 6th Iranian Controlled Release Society Conference CRS. 25th-27th, 2014, Tehran, Iran.
  8. Z. Vatanparast, R. Asgharian, Z. Daman, K. Gilani, S. A. Mortazavi. Preparation and in vitro characterization of spray-dried powder formulations of fluticasone/cyclodextrin complexes for pulmumnary drug delivery.  6th Iranian Controlled Release Society Conference CRS. 25th-27th, 2014, Tehran, Iran.
  9. R. Asgharian, A. Heidari, A. Montaseri, A. Abdollahpour, S. Ghiaee, M. Aminian. Evaluation of efficiency of some disinfectants in disinfection of water treatment system in the pharmaceuitical industry and select the best one. Medicinal Science Journal of Islamic Azad University Vol. 23, No.3, Fall 2013.
  10. A. Mahboubi, M. Kamelinejad, M. Shalviri, Z. Karbasi, Z. Jafariazar, R. Asgharian. Evaluation of antibacterial activity of three Iranian medicinal plants. African Journal of Microbiology Research. Vol. 6(9), pp. 2048-2052, March 2012.
  11. S.V. Taghavian, R. Asgharian, M. Aminian, A. Abdollahpour, A. Montaseri, S.A. Mortazavi, Z. Jafari Azar. Validation of LAL on some antibiotics : a study on the couses of different inhibitory effects. Journal of Pharmaceutical & Health Science. Vol. 1, Jan 2011
  12. K. Mireskandari, R. Asgharian, A. Mahboubi, M. Aminian, S.A. Mortazavi. Comparison of cylindre-plate method in determination of nystatin in vaginal tablets. First Seminar Of “Naghshe Oloume Payeh Dar Erteghae Salamat.” March 2011.
  13. K. Mireskandari, R. Asgharian, A. Mahboubi, M. Aminian, S.A. Mortazavi. Evaluation of factors affecting the potency of nystatin vaginal tablets.  First Seminar Of “Naghshe Oloume Payeh Dar Erteghae Salamat.” March 2011.
  14.  A. Heidari, R. Asgharian, A. Abdollahpour, S.A. Mortazavi. Comparison of cylindre-plate method in determination of nystatin in vaginal tablets. First Seminar Of “Naghshe Oloume Payeh Dar Erteghae Salamat.” March 2011.
  15. R. Asgharian, G. Talaian, A. Abdollahpour, N. Mortazavi, M. Forouhi, A. Montaseri, A. Naserzadeh. Analitical of residue of penicilins (benzyl penicillin, procaine and benzatin) by chemotrapic method for study on cleaning validation in pharmaceutical company. International Symposium on High-Performance Liquid Phase Seperations and Techniques. Budapest-Hungary, Jan 2011.
  16.  R. Asgharian, S.T. Mirbaha, A. Abdollahpour, N. Mortazavi, M. Forouhi, A. Montaseri, A. Naserzadeh. A new method of analysis of streptomycin by HPLC with UV detector for cleaning validation in pharmaceutical company. International Symposium on High-Performance Liquid Phase Seperations and Techniques. Budapest-Hungary, Jan 2011.
  17. A. Vatanara, A. Rouholamini Najafabadi, K. Gilani, R. Asgharian, M. Darabi, A

placket-Burman design for screening of the operation variables in the formation of salbutamol sulphate particles by supercritical antisolvent. J of Supercritical Fluids 40 (2007) 111-116.

  1. A. Rouholamini Najafabadi, R. Asgharian, H. Tajerzadeh, K. Gilani, A. Vatanara, M. Darabi, Influence of mechanical milling time on physicochemical properties and stability of Cefotaxime sodium. DARU, 2007; 15 (1): 27-33.
  2. A. Rouholamini Najafabadi, R. Asgharian, H. Tajerzadeh, K. Gilani, A. Vatanara, M. Darabi, Influence of ball milling time on the characterization and degradation of Cefotaxime sodium. IPSC 2006.
  3. A. Rouholamini Najafabadi, R. Asgharian, H. Tajerzadeh, K. Gilani, A. Vatanara, M. Darabi, Effect of Micronization Method of Active Ingredient and Third Component on Deposition Profiles of Cefotaxime Sodium in Dry Powder Formulations. International Aerosol Conference 2006.
  4. A. Rouholamini Najafabadi, R. Asgharian, H. Tajerzadeh, K. Gilani, A. Vatanara, M. Darabi, The effects of fine lactose as a third component on aerosolizatian of cefotaxime sodium from dry powder formulations. DARU 2006; 14: 155-163.
  5. A. Rouholamini Najafabadi, R. Asgharian, H. Tajerzadeh, K. Gilani, A. Vatanara, M. Darabi, The effect of micronization method on characterization and deposition profiles of different dry powder formulations of cefotaxime sodium. J. DRUG DEL. SCI. TECH., 16 (5)363-368 2005.
  6. A. Rouholamini Najafabadi, R. Asgharian, H. Tajerzadeh, K. Gilani, A. Vatanara, M. Darabi, Evaluation of cefotaxime sodium microparticles for respiratory drug delivery, Res Drug Deliv Europe. (2005) 265-268.
  7. A. Shafiee, Z. Mahmoudi, R. Asgharian. Alkaloids of Papaver Pseudo-Orientale

Population Tarom. J.Sci. IR. Vol 8, No.2 1997.