Pharmacare is a leading generic pharmaceutical company in Palestine with a distinction in quality products distributed locally and globally. Our GMP standards, quality research and technical development capabilities, give rise to the illustrious standing the company has been reputed to reflect. Through both internal collaborations and in partnership with external parties, Pharmacare currently prides on depicting a team of quality researchers, nationally and internationally, with the potential to produce quality research in contribution to the ongoing wave of medical and pharmaceutical development.
Publications
- Ghanem M, Abu-Lafi S, Karaman R , Hallak H (2012) , Validated HPLC Method to Simultaneously Determine Amprolium Hydrochloride, Sulfaquinoxaline Sodium and Vitamin K3 in A.S.K Powder on ZIC-HILIC Column, Journal of Pharmaceutica Analytica Acta, Volume 3, Issue 7, 3:168.doi:10.4172/2153-2435.1000168.
- M. M. Ghanem and S.A. Abu-Lafi (2012) , Development and Validation of a Stability-Indicating HPLC Method for the Simultaneous Determination of Sulfadiazine Sodium and Trimethoprim in Injectable Solution Formulation , Scientia Pharmaceutica, Vienna Austria, http://dx.doi.org/10.3797/Scipharm. 1210-12.
- M. M. Ghanem and S. A. Abu-Lafi (2013) , Validation of a Stability-Indicating RP-HPLC Method for the Simultaneous Determination of Trimethoprim and Sulfadimethoxine Sodium in Oral Liquid Dosage Form,Scientia Pharmaceutica, Vienna Austria, http://dx.doi.org/10.3797/Scipharm. 1212-30.
- M. M. Ghanem, S. A. ABU-LAFI, H.O. HALLAK (2013) , Validation of a Stability-Indicating Hydrophilic Interaction Liquid Chromatographic Method for the Quantitative Determination of Vitamin K3 (Menadione Sodium Bisulfite) in Injectable Solution Formulation, Scientia Pharmaceutica, Vienna Austria,http://dx.doi.org/10.3797/Scipharm. 1303-05.
- Mashhour Ghanem, SALEH ABU-LAFI, DIYAA MOHAMMAD (2013), Validated and stability indicating HPLC method for the simultaneous determination of Sulfadiazine sodium, Sulfathiazole sodium and Sulfadimidine sodium in water soluble powder dosage form, International Journal of Pharmacy and Pharmaceutical Sciences ,Int J PharmPharm Sci, Vol 5, Suppl 3, 547-554.
- Mashhour Ghanem, SALEH ABU-LAFI (2013), Validation of a Stability-Indicating Assay of Amprolium Hydrochloride in Water Soluble Powder Formulation using Hydrophilic Interaction Liquid Chromatography, Journal of Applied Pharmaceutical Science Vol. 3 (10), pp. 051-058.
- Mashhour Ghanem, SALEH ABU-LAFI, DIYAA MOHAMMAD (2014), Development and validation of a stability-indicating hydrophilic Interaction liquid chromatographic method for the determination of Sulfaquinoxaline sodium in water soluble powder formulation, International Journal of Pharmacy and Pharmaceutical Sciences ,Int J Pharm Pharm Sci, Vol 6, Suppl 2, 652-657.
- Abdel Naser Zaid, PhD, Mohyeddin Assali, Aiman Qaddomi, Mashhour Ghanem, Yara Abu Zaaror (2014), preparation and stability evaluation of extemporaneous oral suspension of valsartan using commercially available tablets , International Journal of Pharmaceutical Compounding, Vol 18, No.2,169-174.
- Mashhour Ghanem, SALEH ABU-LAFI, (2015),Development and Validation of RP-HPLC Method for the Simultaneous Determination of Trimethoprim, Sulfadimidine Sodium and Tylosin Tartrate in injectable solution formulation, Journal of Applied Pharmaceutical Science , Vol 5 (1), Suppl 2, 094-098. 10. Abdel Naser Zaid, Aiman Qaddomi, Mashhour Ghanem, Lina Shehadeh, Murad.
- Abdel Naser Zaid, Aiman Qaddomi, Mashhour Ghanem, Lina Shehadeh, Murad Abualhasan, Salam Natur, and Saed Khammash (2015), Development of a Dissolution Method to Compare Tablet Formulations Containing Valsartan /Amlodipine ,Dissolution Technologies, Vol 22 Issue 3, 32-38.
- Murad Abualhasan, Mashhour M. Ghanem, Mohyeddin Assali, Abdel Naser Zaid ,(2015), The effect of non-compliance of PPI instruction on the stability of reconstituted oral antibiotics, Journal of Applied Pharmaceutical Science , Vol 5 (08), Suppl 2,143-146.
- Ramzi Shawahna, Mashhour Ghanem, Ayat Ghanem, Abdul-fattah Mansour, Nema Ahmad and Abdel Naser Zaid (2015), Establishing similarity between multisource Betahistine Dihydrochloride oral dosage forms using in vitro methods, Acta Poloniae Pharmaceutica ٌ Drug Research”, Vol. 72 No. 6 pp. 1245-1252.
- Zaid AN, Ghanem M, Maqboul L, Zaid H, Mahasne A (2016), Biowaiver Eligibility of a Lower Strength Ramipril/Hydrochlorothiazide Immediate Release Tablets Using a New Validated HPLC Analytical Method, Georg Thieme Verlag KG Stuttgart.
- Abdel Naser Zaid , Mashhour Ghanem, Dua’a Shweiki , Hala Shtewi ,Raja Shaheen, Sondos AL-Helaly Zeina Khayyat Rowa Alramahi, Saed H Zyoudi (2016), In vitro and in vivo postmarketing surveillance of valsartan, alone or in combination with amlodipine or hydrochlorothiazide, among Palestinian hypertensive patients, Therapeutics and Clinical Risk Management, DovePress.
- Abdel Naser Zaid, Nihal Zohud, Tasneem Aburadi, Aiman Qaddomi, Yara Abu Zaaror, Bushra E’Layan, Nidal Jaradat, Iyad Ali, Fatima Hussein, and Mashhour Ghanem, “Pharmacodynamic testing and new validated HPLC method to assess the interchangeability between multi-source orlistat capsules,” Drug Design, Development and Therapy, vol. 11, pp. 3291–3298, 2017.
- Abdel naser Zaid , Rania Shtayah , Ayman Qadumi, Mashhour Ghanem, Naim Kittana, Stability of extemporaneously prepared rosuvastatin oral suspension, American Journal of Health-System Pharmacy 74(19):1579-1583 · October 2017, DOI: 10.2146/ajhp16023
- Formulation and bioequivalence of two Valsartan/Amlodipine Immediate release tablets after a single oral administration Abdel Naser Zaid*1, Salam Natur2, Aiman Qaddomi2, Murad Abualahasan1, Rowa Al- Ramahi1, Naser Shraim1, Saed Khammash1 and Nidal Jaradat1
- Formulation and bioequivalence of two Valsartan/Amlodipine Immediate release tablets after a single oral administration Abdel Naser Zaid*1, Salam Natur2, Aiman Qaddomi2, Murad Abualahasan1, Rowa Al- Ramahi1, Naser Shraim1, Saed Khammash1 and Nidal Jaradat1
- Formulation and in vitro and in vivo evaluation of film-coated Montelukast sodium tablets using Opadry® yellow 20A82938 on an industrial scale Abdel Naser Zaid1, Salam Natur2, Aiman Qaddumi2, Abeer Abu Ghoush1,
- Weight and content uniformity of lorazepam half-tablets:A study of correlation of a low drug content product Abdel Naser Zaid a,*, Rowa’ J. Al-Ramahi a, Abeer Abu Ghoush a, Aiman Qaddumi b, Yara Abu Zaaror b
- Comparative Bioavailability of Two Ciprofloxacin XR Formulations in Middle Eastern Healthy Volunteers After a Single Oral Administration. Abdel Naser Zaid a, Ayman Qaddumi b, Saed Khammash
- Development and stability evaluation of enteric coated Diclofenac sodium tablets using Sureteric Abdel Naser Zaid and Aiman Qaddomi1
- Formulation of bifonazole powder and development of a new stability indicating HPLC method for its analysis Abdel Naser Zaid, Ayman Qaddomi, Saed Khammash
- Comparative Bioavailability of Two Cefdinir Suspension Formulations in Middle Eastern Healthy Volunteers after Single Oral Administration Abdel naser Zaid, Franco Alhaique, Jamal Kort, Prof. Waleed Sweileh
- Comparative Bioavailability of Two Cefdinir Suspension Formulations in Middle Eastern Healthy Volunteers after Single Oral Administration Abdel naser Zaid, Franco Alhaique, Jamal Kort, Prof. Waleed Sweileh