Journal of Developing Drugs
Open Access

4^th International Summit on GMP, GCP & Quality Control

October 26-28, 2015 Hyderabad, India

Scientific Tracks Abstracts

• Entropy in good manufacturing practices driven by innovative quality tool for pharmaceutical industry: New paradigm approach for manufacturing excellence and quality standards

  Pradeep K Jha1, 2, Rakhi Jha1 and Sujoy K Guha1,2

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• Comparison of guidelines of Indian GMP with WHO GMP

  Uma Vasireddy

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• Role of ‘c’ in cGMP

  Abha Doshi

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• Clinical documentation supporting core labels for generics/OTC products

  Aswin Kumar Allupati

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• Quality management systems

  Vaishali P Nagulwar

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• Current GMP guidelines

  Abha Doshi

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• Comparison of regulatory requirements for marketing authorization of biologics in United States and European Union

  Shashi Kumar Yadav

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• Food safety management systems: Requirements for any organisation in the food chain (ISO 22000:2005)

  R Manavalan

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• HPLC method development and validation as per ICH guidelines

  Arunadevi S Birajdar

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• Identification of biomarker(s) from polyherbal formulation used in hyperlipidemia for qualitative and quantitative analysis

  Charmy S Kothari, Maulik Ranpariya and Priti Mehta

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• Almighty Astaxanthin: Over view on nutraceutical based approach to aim to combat cancer

  Kandra Prameela, Ch Murali Mohan and K P J Hemalatha

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• Effective GMP audits for APIs and formulation in pharma companies

  G Sundar

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• Pharmaceutical process validation: A tool for pharmaceutical compliance monitor

  Sheelpriya Ratnakar Walde

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• Quality control analytical methods - Switch from HPLC to UPLC

  Y Padmavathi

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• How to prevent outbreaks in endemic countries?

  Ravi Kumar Tummalacharla

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• Studies on β-CD complexation of a poorly soluble drug

  Mohidurakshan1, Nisar Ahmad Khan2 and Khalid Bashir Mir2

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• Solubility and dissolution rate enhancement of Aceclofenac by solid dispersion technique

  Khalid Bashir Mir1,Nisar Ahmed Khan2 and Mohi Durakshan2

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• Good manufacturing practice (GMP): An overview

  Firoj A Tamboli and H N More

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• A validated UPLC/ESI-MS/MS bio-analytical method for the quantification of Perindopril and Amlodipine in human plasma

  Kalaiyarasi Duraisamy

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• Adverse drug reaction reporting: A retrospective analysis

  Ibel C Fredy

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• 3G system in pharmacy practice with vigilance

  Khwaja Amtul Raouf Qazi

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• Data mining – De-Novo quality management tool in food sector

  S Thiruchenduran

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• Zebrafish as a model system for drug target screening and validation

  Bhusnure O G, Gholve S B, Mane J M, Giram P S and Thonte S S

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• Estimation of Ramelteon in bulk and tablet dosage form by HPLC

  Varaprasad Adepu

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• QbD approach for the development and optimization of HPLC method for the simultaneous estimation of four component cream formulation: Application to permeability study

  Prachi Bhamre, Madhuri Baghel and Sadhana J Rajput

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• Good Clinical Practice (GCP) and declaration of helsinki

  Pooja Roy

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