Journal of Developing Drugs
Open Access

3^rd International Summit on GMP, GCP & Quality Control

September 25-26, 2014 Valencia Convention Centre, Spain

Accepted Abstracts

• Essentials in quality by design

  Thomas A Little

  PDF HTML

• Planning to outsource manufacturing: Have you done your homework?

  Mohammed R Khan

  PDF HTML

• A guide to an effective clinical trial protocol in cGMP & cGCP as a tool for sustenance of ethical principles and regulatory requirements in the pharmaceutical and research industry

  Peter Odeh and Helen Odeh

  PDF HTML

• The process validation approach in the 21st century

  Paul F O Otieno, Omwalo, G Obiero and V Nyamthimba P NdubaV

  PDF HTML

• Comparative evaluation of biomarker psoralenin antioxidant active extracts of different species of genus Ficus by validated HPTLC method

  A l Ajmi Mohamd F and Alam P

  PDF HTML

• Quality control and lean management: A holistic concept of building quality and cost reduction in a manufacturing enterprise

  Akintunde and A Sowunmi

  PDF HTML

• Qualifying pharmaceutical excipient suppliers: The role of EXCiPACT™

  Allan Whiston

  PDF HTML

• Preventive effects of crocin against hepato cellular carcinoma

  Amr Amin and Sayel Daoud

  PDF HTML

• Efficacy enhancement of hydrophobic antibiotics employing rhamnolipid as biosurfactant

  Abdurrahim A Elouzi, Abdurrauf M Gusbi and Ali M Elgerbi

  PDF HTML

• Good practices on pharma distribution: A case study

  Bruno Guella

  PDF HTML

• Prescription pattern of psychotropic medicines at a neuropsychiatric hospital in Nigeria; A drug utilisation study

  Charles C Ezenduka, Vincent N Ubochi and Brian O Ogbonna

  PDF HTML

• Reference standards for quality control

  Cornelia Horoiu

  PDF HTML

• Toxicological assessment of degradation products: Is it relevant as a complementary approach during stability testing of pharmaceuticals?

  Daniele Rubert Nogueira

  PDF HTML

• From a training perspective: What does the FDA look for during an inspection?

  David Gallup

  PDF HTML

• Rates and types of prescribing errors and related interventions in oncology

  Nessrin Ahmed El-Nimr

  PDF HTML

• Efficiency in the context of data quality: The role of design and technology

  Vikram Kukkadi

  PDF HTML

• Acquired error in using antibiotic for surgery patients in Iraqi hospitals

  Fadya Y Alhamdani

  PDF HTML

• Variability and stability of bread and durum wheat for phytic acid content

  Gordana Surlan-Momirovic, Gordana Brankovic, Vesna Dragicevic, Dejan Dodig, Miroslav Zoric, Desimir Knezevic and Srbislav Dencic

  PDF HTML

• Minimization and optimization of water use in the process of cleaning containers

  Hanane El Asslani

  PDF HTML

• Novel drug delivery systems

  Hossein Mostafavi

  PDF HTML

• Current restructuring ordeal & the future ahead for CMOs

  Kamaljit Behera

  PDF HTML

• Plant-based expression of pharmaceutical proteins to improve global health

  Kathleen L Hefferon

  PDF HTML

• Knowledge management

  Lothar Hartmann

  PDF HTML

• Pharmaceutical quality system

  Lothar Hartmann

  PDF HTML

• Setting acceptance criteria for validation of analytical methods of drug eluting stents: Minimum requirements for analytical variability

  Marika Kamberi

  PDF HTML

• Heavy metals body burden and evaluation of human health risks in African catfish (Clarias gariepinus) from Imo River, Nigeria

  Pereware Adowei and Michael Horsfall Jr

  PDF HTML

• Best quality practices for biomedical research in drug development

  Michele Luke Pruett

  PDF HTML

• Molecular modeling design, synthesis and antihyperglycemic evaluation of certain 5-(arylalkoxybenzylidine)- imidazolidine-2,4-dione derivatives as potential PPARγ agonists

  Michelyne Haroun and Christophe Tratrat

  PDF HTML

• Integration lean and six sigma to improve the performance of corrugated fiber board “C.F.B.” manufacturing

  Mohamed Ibrahim Zaki Ibrahim

  PDF HTML

• Medical devices regulations in Southeast Asia: Example of Malaysia

  Mourad Kholti

  PDF HTML

• Have you taken a look at your training quality system lately? Ever?

  Graelynn McKeown

  PDF HTML

• Training and education the WHYs of cGMP to operators can make a huge difference in meeting CQV standards inside pharmaceutical manufacturing facilities

  Susan Stipa

  PDF HTML

• The right training, the right people, the right time

  Bella Graffam

  PDF HTML

• Cost of poor quality in a pharmaceutical industry: A case study

  Muhammad Jawad Bhatti and Muhamamd Usman Awan

  PDF HTML

• Cleaning validation for halal pharmaceutical industry

  Nizamil Fairuz Yahya

  PDF HTML

• Industrial design: Disrupting the established protocol in the pharmaceutical and medical device research and development

  Oscar J Acosta

  PDF HTML

• Influence of process parameters on tablet bed micro environmental factors during pan coating

  Preetanshu Pandey, Dilbir S Bindra and Linda A Felton

  PDF HTML

• Art of GMP auditing - for auditor and auditee

  Ralf Bradenahl

  PDF HTML

• GMP compliance for inspections, sampling and testing of packaging components in pharmaceuticals

  Sarma R Donepudi

  PDF HTML

• Historical developments of Good Manufacturing Practices

  Sreenivasa Rao Bantupalli

  PDF HTML

• Sterile/Aseptic manufacturing: Additional challenges in production of radiopharmaceuticals

  Valentina Ferrari

  PDF HTML