Pharmaceutical Regulatory Affairs: Open Access

Titel Veröffentlichungsdatum Sprache Zitate
Europe - New regulations - What impact will the proposed new regulations in Europe have for medical device manufacturer?2013/01/014
E-pharmacies Regulation in India: Bringing New Dimensions to Pharma Sector2016/01/013
Medical Devices Regulation in United States of America, European Union and India: A Comparative Study2017/01/013
Ever-greening in Pharmaceuticals: Strategies, Consequences and Provisions for Prevention in USA, EU, India and Other Countries2017/01/013
The Use of Medicinal Plants in Human Healthcare: A Scoop on Safety2014/01/013
Is SteradR from J&J is Truly Plasma Gas Sterilizer?2014/01/013
Regulations on Adaptive Design Clinical Trials2014/01/013
Screening of Compounds from an FDA-Approved Drug Library for the Ability to Inhibit Aspartic Protease Secretion from the Pathogenic Yeast Candida albicans2014/01/013
Post Marketing Surveillance of Anti-malarial Medicines in Tanzania2017/01/013
Current Mistaken Interpretation of Microbiological Data on Gas Plasma Sterilization2015/01/012
Comparison on Safety Concern Among Gamma-Ray, Autoclave and Ethylene Oxide Gas Sterilizations of Thermosetting Polyurethane2014/01/012
Health Hazards in the Pharmaceutical Industry2015/01/012
Responsibility of Regulatory Affairs in Pharmaceutical Industry2016/01/012
Harmonized Guideline on Limit and Testing of Elemental Impurities in Pharmaceutical Substances: A Review2016/01/012
Simultaneous RP-HPLC Method Development and Validation of Atorvastatin, Ezetimibe and Fenofibrate2016/01/012
Development of Innovative Medicines for European Patients and Impact of Brexit2016/01/012
Biosimilars: an Emerging Market Opportunities in India2016/01/012
Pharmaceutical Good Manufacturing Practice Regulatory Affairs in Sudan: Continuous Debate between Regulatory Authority and Manufacturers2016/01/012
Simultaneous Achievement of Sterility Assurance Level (SAL) of 10-6 and Material and Functional Compatibility in Gas Plasma Sterilization2015/01/012
FDA Regulation of Medical Devices and Medical Device Reporting2013/01/012
Novel Drug Therapies and Diagnostics for Personalized Medicine and Nanomedicine in Genome Science, Nanoscience, and Molecular Engineering2012/01/012
The Retail Pharmacy Market in the Brazilian Federal District2015/01/011
Drug Review Differences across the United States and the European Union2015/01/011
VDAC as a Potential Target in Huntingtons Disease Therapy: The State of the Art2015/01/011
Transfer behavior of the weakly acidic BCS class II drug valsartan from the stomach to the small intestine during fasted and fed states2018/01/011
Electrochemical Detection versus Ultraviolet Detection2014/01/011
Problems of enforcements of regulations on pharmaceutical industry in Bangladesh2014/01/011
Role of Essential Drug List in Effective Management of Essential Anti- Malarial Drugs in Healthcare System of Pakistan Challenges in Policy Development to Practice2014/01/011
Solid Lipid Nanoparticle: An Overview2015/01/011
Regulation of Herbal (Traditional) Medicinal Products in the European Union2015/01/011