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Regulatory affairs for healthcare products
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European regulatory framework for drug approval through the centralized system
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Pre-analytics- a challenge less heeded
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Patents in Indian pharmaceutical industry: Legal and ethical issues
B. S. Kuchekar
Crystallization in the pharmaceutical industry
Balbir Negi
Bapurao B. Shingate
Formulation and evaluation of fast disintegrating sublingual tablets of Rizatriptan
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D L Sharma
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Medication errors in pediatric population: Magnitude and interventions
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Devinder Pal
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Complimentary approaches to metabolic syndrome: Opportunities and challenges
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Understanding facility validation for GMP compliance
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Cassia occidentalis: Effect on skin wound healing in mice induced by Bootrops moojeni venom
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Manthan D Janodia
Overcoming the challenge of differing guidelines for compliance with GMP by different authorities
Mithilesh Trivedi
Mohammad Shahbaz Alam
Developing regulatory environment in South Asia and challenges for regulatory affairs professionals
Nadeem H. Alamgir
Corrective action & preventive action (capa system) and regulatory inspection
S N Kilikar
Naveen Kulkarni
Design and synthesis of novel antifungal peptides and their mode of action
Rajendra Prasad, Indresh Kumar Maurya and Virander Singh Chauhan
Raman Dang
Sambasivarao Kotha
Sandeep Arora and Arvind sharma
SGLT-1: A Novel target for drug development in cardiomyopathy and heart failure
Sanjay K Banerjee
Optimising the bang for buck in the realm of therapeutic ontology using patent and XP documents
Sankar Sundaram and Shubhankar Joshi
Cool clot, a novel haemostatic agent for controlling life-threatening arterial bleeding
SMJ Mortazavi
Hybridization strategies in the development of anti tubercular agents
Srinivas Kantevari
How does quality impact business success
Sunita Sharma
Quality assurance of herbal medicinal products: Past, present & future
Tejal R. Gandhi
U.K. Patil
1, 2, 3-Triazoles as Pharmacophores
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Highly facile chemoenzymatic synthesis of complex sialic acids
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Stable biocompatible silver nanoparticles (w/o) cream for safe, better and empiric wound healing
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Pharmaceutical outsourcing: An upward trajectory
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Formulation and evaluation of anti-migraine controlled release microspheres of sumatriptan succinate
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Affect of foreign direct investment on host countries
Ashok
Ethical issues in vaccine clinical trials
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Microbivores: Artificial mechanical phagocytes using digest and discharge protocol
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The regulations of import and sale of the pharmaceutical product in Vietnam
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K. Ludajic and J. Hicks
Analytical software for clinical trials
K. Ramesh Kumar1 and Swetha G
Regulatory frame work for biosimilar monoclonal antibodies
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Sonal Srivastava, Kapil Verma and Jyoti Singh
Regulatory strategy for similar biologics in India
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Simultaneous spectrophotometric estimation of gemifloxacin and ambroxol from tablet formulation
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Formulation and evaluation of diclofenac sodium gels using carbopol and hpmc as gelling agents
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Nanogel: A novel tool for controlled drug delivery system
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ANDA Suitability Petition vs. 505 (B) 2 Applications
Pandya Hardik P
Poonam Verma
Solubility enhancement techniques
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Impact of pharma regulations on pharmaceutical economy
Prathyusha. A
Priya Prasad
Optimization of inducer concentration in the medium for production of glutaminase from Erwinia
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Formulation and evaluation of oral disintegrating tablets of sumatriptan succinate
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Bioinformatics, drugs & omics- An overview of the major areas of the omics
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Evaluation of Sterotex HM in optimization of curcumin loaded solid lipid nanoparticles
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Sedative, anxiolytic and analgesic effects of the methanol extract of Urena sinuata L.
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Sanjay Reddy Akula and Jyothi Edla
A novel drug delivery system: Insulin free needle injection technology
Sanjay Reddy Akula and Jyothi Edla
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Saurabh Maru, G Mugesh and B C Das
Shahana Sharmin, Nuzhat Mariam Elias and Ishtiaq Ahmed
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Sravani Yarlagadda
Optimization of the lyophilization cycle by using process analytical technology
Sreedhar Bandari
Senthil Balan S and Jayalakshmi S
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Teegala Suraj Benarji
Formulation and evaluation of floating drug delivery system of poorly soluble drug
Suryakant Gupta, Gupta A. P and Sharma M
Talha Bin Emran
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Good Automated Manufacturing Practice (GAMP)
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Divya Sree, Thadkapally Srinivas and Aramalla Eashwar Rao
Stability-indicating HPLC method for quantification of valsartan in pharmaceutical dosage forms
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Design and development of matrix type hydroxyzine hydrochloride transdermal patches
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Adverse drug reaction-causality assessment scales
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Stability-indicating HPLC method for Quantification of Valsartan in pharmaceutical dosage forms
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Design and development of matrix type hydroxyzine hydrochloride transdermal patches
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Pharmaceutical Regulatory Affairs: Open Access received 533 citations as per Google Scholar report