Follow
Pharmaceutical Regulatory Affairs: Open Access
Pharmaceutical Regulatory Affairs: Open Access
Editor
Verified email at pharmajournals.org
Title
Cited by
Cited by
Year
Malaysian cosmetic market: Current and future prospects
MA Hassali, SK Al-Tamimi, OT Dawood, AK Verma, F Saleem
Pharmaceutical Regulatory Affairs 4 (4), 1-3, 2015
1072015
Antibiotic abuse in developing countries
R Abdulah
Pharm Regul Aff 1 (2), 1000e106, 2012
652012
Death after quadrivalent human papillomavirus (HPV) vaccination: causal or coincidental
L Tomljenovic, CA Shaw
Pharmaceut Reg Affairs S 12, 2, 2012
392012
Micellar solubilization in the formulation development of poorly soluble naproxen
PD Maheswari, D Rambhau, ML Narasu
Pharm Reg Affairs 2 (108), 2, 2013
212013
The three-level approach: a framework for ensuring medicines quality in limited-resource countries
VS Pribluda, A Barojas, V Coignez, S Bradby, Y Dijiba, L El-Hadri, ...
Pharmaceut Reg Affairs 3 (1), 117, 2014
202014
Biosimilars: an emerging market opportunities in India
P Rushvi, K Charmy, C Nirav, C Narendra
Pharmaceut Reg Affairs 5 (1), 1-7, 2016
172016
Harmonized guideline on limit and testing of elemental impurities in pharmaceutical substances: a review
MM Reddy, KH Reddy, MU Reddy
Pharmaceut Reg Affairs 5 (2), 1-8, 2016
172016
Pharma regulations for generic drug products in India and US: case studies and future prospectives
S Swain, A Dey, CN Patra, ME Bhanoji Rao
Pharmaceut Reg Affairs 3 (119), 1-6, 2014
162014
FDA regulation of medical devices and medical device reporting
N Teow, SJ Siegel
Pharmaceut Reg Affairs 2 (110), 2, 2013
142013
The use of medicinal plants in human healthcare: a scoop on safety
M Eddouks, D Ghanimi
Pharm Regul Aff 3 (1), 1-21, 2013
142013
Marijuana toxicity: heavy metal exposure through state-sponsored access to “la Fee Verte”
DV Gauvin, ZJ Zimmermann, J Yoder, R Tapp
Pharm. Regul. Aff. Open Access 7, 1-10, 2018
132018
Impact of API (active pharmaceutical ingredient) source selection on generic drug products
UR Mallu, AK Nair, J Sankar, HR Bapatu, MP Kumar, S Narla, TA Bhanap, ...
Pharmaceut Reg Affairs 4 (2), 11, 2015
132015
Drug review differences across the United States and the European Union
MM Sifuentes, A Giuffrida
Pharmaceut Reg Affairs 4, e156, 2015
132015
Patient Compliance: An Untold Story or a Fairy Tale
AK Mohiuddin
Pharmaceut Reg Affairs 7 (2), 207, 2018
92018
Regulatory requirements and drug approval process in India, Europe and US
AM Sawant, DP Mali, DA Bhagwat
Pharmaceut Reg Affairs 7 (210), 2, 2018
82018
Health and beauty cosmeceuticals industry and market expansion in Saudi Arabia
E Tambo, H Almeer, Y Alshamrani
Pharmaceut Reg Affairs 5 (172), 2, 2016
82016
Pharmaceutical good manufacturing practice regulatory affairs in Sudan: continuous debate between regulatory authority and manufacturers
A Abedellah, M Noordin, AA Zaki
Pharmaceut. Reg. Affairs 5 (166), 2, 2016
82016
Current regulatory scenario for conducting clinical trials in India
B Ramu, M Sathish Kumar, M Ramakrishna
Pharmaceut Reg Affairs 4 (2), 1-3, 2015
82015
Impact of pharmacovigilance in healthcare system: regulatory perspective
S Swain, CN Patra
Pharmaceut Reg Affairs 3 (5), 2014
82014
Non-equivalence of antibiotic generic drugs and risk for intensive care patients
C Kirkpatrick, R Ramzan, R Mykhaylo, B Mike, G Shahram
Pharmaceut Reg Affairs 2 (1), 1-7, 2013
82013
The system can't perform the operation now. Try again later.
Articles 1–20