Journal of Developing Drugs
Open Access

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

October 26-28, 2015 Hyderabad, India

Posters-Accepted Abstracts

• New RP-HPLC method for the determination of Afatinib dimaleate in bulk and pharmaceutical dosage forms

  Ravikumar Vejendla1, C V S Subramanyam2 and G Veerabhadram3

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• A brief analysis of regulatory structure and approval process of pharmaceuticals in GCC

  K Vamshi Kumar, Shashi Kumar, Chandra Shekar and A Sambasiva Rao

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• Study on the registration requirements of generic applications in Latin American countries (Venezula, Chile, Colambia, Peru, Argentina & Mexico)

  Md Amer Mohioddin, Shashi Kumar, P Srinu and A Sambasiva Rao

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• Regulatory requirements for generic drugs (ANDS) in Canada

  R Rajender, Shashikumar Yadav, P Prudhvi and A Sambasiva Rao

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• Cleaning validation: Methods to determine residue of cleaning agents

  T Bhaskar, Shashi Kumar and A Sambasiva Rao

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• Importance of cGMP in pharmaceutical industries

  B Poornima, B Nagarani and D Karthikeyan

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• Good practice for the management of quality audits conducted by regulatory audits

  D Ravali Reddy, Shashi Kumar, Sanjeev Kumar and A Sambasiva Rao

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• Process validation and its regulatory requirements according to USFDA, ICH, GHTF

  A Divya, Shashi Kumar, T Mamatha and A Sambasiva Rao

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• A review on good manufacturing practices for medicinal productions

  Divya Dhatri Kara

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• Regulatory requirements of stability studies

  J Srilatha, Shashi Kumar, Geetha and A Sambasiva Rao

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• Regulation of pre-clinical & clinical trial approval process in ASEAN countries

  Saba Fatima, Shashi Kumar, D Sumathi and A Sambashiva Rao

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• HACCP application in bulk cream and butter industries: A review

  Sindhuja S, Veena G and Sreevalli M V

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• Comparison of regulatory requirements for the submission of dossier to South Africa (ZA-CTD) and ASEAN (ACTD)

  V Sreevalli, Shashi Kumar Yadav, Krishnanjali and A Sambasiva Rao

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• Question based review for generic drug for regulatory compliance in US

  A Swetha Kumary, Shashi Kumar Yadav, P Haritha and A Sambasiva Rao

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• Role of quality assurance in warehouse activities for the compliance of GMP

  Veena G, Shashi Kumar and A Sambasiva Rao

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• Analysis of cephalosporin antibiotics in the pharmaceutical dosage forms using ultra performance liquid chromatography instrument

  Satish Pavuluri, Sridhar Siddiraju and Rajesh V

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• A validated stability-indicating RP-HPLC assay method for the determination of Zaltoprofen

  Pranathi Garika, Lahari, Srivani and Shankar

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• Targeted therapy by calypso 4D localization system

  Gayathri Vyshalini and Swapna

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• Cytotoxicity and pulmonary toxicity evaluation of engineered carbon nano-rods in human cell lines and rats

  Ajay Kumar, Durgaiah and Narsimha

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• Development and validation of single analytical method for the simaltaneous estimation of nine drugs proton pump inhibitors and their combinations with prokinetic agents and non-steroidal anti inflammmatory drugs

  Vijayalakshmi Atla and Gowri Sankar Danana

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• Clinical trials registries towards improved access to therapeutic data

  V Keerthi Chandana

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• Clinical trials: Footprint to the future

  G Satya Sravani

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• RP-HPLC method development and validation for evaluation of drug residue after cleaning of equipments of ointment formulation

  Monika S Sonawane

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• Good Automated Manufacturing Practices: A master control process for manufacturing in pharmaceutical industry

  Swapneel Hari Bagal1, Geeta Parasnath Darekar

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• Good Manufacturing Practices: The Gap within

  Derle Nikita Diliprao1, Derle Deeliprao Vishramji2, Sonawane Monica Shivaji3

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• Overview of data integrity in the pharmaceutical laboratory and current regulatory challenges

  Abhay Gupta

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• Chemical and pharmaceutical analysis, stability and dissolution studies of drugs and medicines: Quality control of drugs and medicines

  Edith Cristina Laignier Cazedey

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• P-CHECK: A safety checklist for a chronic pain service

  Emanuele Piraccini

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• Good manufacturing practices and globalization

  Gannu Praveen Kumar

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• Challenges in analytical method development of biopharmaceuticals

  Kalyana Sundaram R

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• Quality by design in pharmaceutical quality control analysis: Tool for regulatory flexibility

  M V Narendra Kumar Talluri

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• Virtual clinical trials in Asia: A new study paradigm for the future?

  Miguel Orri

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• Bioactive compounds from natural product to pharmaceutical industry: GMP via GLP

  Reeta Mandal1, 2, 3

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• Prometeo: Epidemiological registry for chronic pain

  Silvia Ussai

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• Applications of good manufacturing practices (GMP) and hazard analysis and critical control point (HACCP) system in hygienic chicken meat production at retail level

  Subhasish Biswas1, 2

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• Automated storage and retrieval systems (ASRS) in India: Application outlook on chemicals/ pharmaceutical industries

  Yash Parikh

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• Challenges in implementing good clinical practice (GCP) guidelines and their mitigations

  Vineela Nekkanti

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• Upgradation of Punjab veterinary vaccine institute, Ludhiana as per GMP norms

  Pritpal Singh and Kulwant Singh

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• Readiness for regulatory inspection and audits

  Neerja S

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• Good laboratory practices: A wake up call for pharmaceutical industries

  Prakash V Diwan1, 2 3, 4, 5

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• Effects of lean manufacturing practices to encourage continuous improvement for manufacturing excellence

  Dharmvir Uppal

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• Quality control methodologies for standardization of herbal medicines: An assessment

  Raja Chakaverty and Amitava Ghosh

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• Indian clinical trials- The unaddressed challenges of regulatory amendment

  N Srinivas

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• HPLC fingerprinting for quality control of herbal drugs

  Nutan Kaushik and Daya Bhardwaj

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