Journal of Developing Drugs
Open Access

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

September 25-26, 2014 Valencia Convention Centre, Spain

Scientific Tracks Abstracts

• Regulatory requirements and benefits converting to continued process verification

  Magnus Jahnsson

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• Greening the pharmaceutical industry to afford Good Laboratory Practice

  Salwa Elmeligie

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• Effective methods for software and systems integration for software companies and institutions

  Boyd L Summers

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• Reflections about Quality Control and Quality Assurance in clinical trials

  Fernando Geijo

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• Role of Good Laboratory Practice in Good Clinical Practice

  Salwa Elmeligie

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• Quality excellence through benchmarking quality improvement models

  Kamran Atif

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• Ensure quality assurance for software companies and institutions

  Boyd L Summers

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• Effective CAPA Program, A valuable tool in quality improvement

  Dharmi Trivedi

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• Evaluation of bacterial contamination of clean room clothing

  Noelle H O Driscoll, Laurie Smith, Mary Tully, Hannah Prescott and Andrew J Lamb

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• Optimization solutions for validation procedures in the quality control of enantiomers; Chirality tests for antidepressants Citalopram and Venlafaxine

  Ivanka Pencheva, Lily Peykova and Genka Petrova

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• How to improve quality and consistency of legacy products applying QbD/Six Sigma methodology

  Alicia Tebar

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• Maintain the effectiveness of a QMS by using Lean Six Sigma approach

  Peter Jehander

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• Analytical method lifecycle management

  Gerald de Fontenay

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• Managing equipment validation using ASTM approach for optimum cost and aggressive schedule

  Sundar Chellamani

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• Industrial process validation of metformin tablets to facilitate the scale up of commercial production: A GMP and validation perspective

  Gannu Praveen Kumar and Bela Manohar

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• GMP system implementation and certification to manufacture seawater ampoules as a dietary supplement under ISO 5 air quality

  Maria Pellin Amoros

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• DHF, DMR and DHR - The three Ds of Medical devices

  Rama K Pidaparti

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• Assessing pharmaceutical equipment containment using surrogate monitoring (SMEPAC)

  Mootaz El Halawani

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• Challenges of cGMP implementation at different CMO’s - Role of quality agreements

  Rivka Zaibel

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• CMO’s challenges and strategies in sterile manufacturing

  Jixing Wang

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• Production of biosimilars in developing countries: Challenges and opportunities: SEDICO case Study

  Wael Ebied

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• The relevance of training in supply chain management of pharmaceutical products

  Ibelema Emeh

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