Global Bio-Clinical Trials

Organization: CPhI Conferences India

Event Date/Time: Nov 21, 2012 / 9:00 am - (GMT +5:30 hours) End Date/Time: Nov 23, 2012 / 5:00 pm - (GMT +5:30 hours)
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Our expert speakers will provide you with implementable and vital solutions for navigating through complex domestic, developed and emerging market regulations along with optimal design and execution of your bio-clinical trials.    
Exclusive! One day Seminar on Regulatory Framework in Emerging Markets :
Implement best practices to ensure flawless execution of ambiguous and complex regulatory guidelines in emerging markets to have the first mover advantage of your products in Brazil, Russia, China, Malaysia and LATAM
Conference Highlights:

Conference Day 1 Conference Day 2
  • Indian Regulatory Landscape- DCGI &ICMR
  • US-FDA and EMEA norms for clinical trials
  • Comparative Trial Studies
  • Role of Ethic Committees
  • Design of Clinical trials
  • Immunogenicity
  • Patient Recruitment & Retention
    Dr Ragunadarao Digumarti, HOD, Oncology,
NIZAMS Hyderabad

  • Clinical Data Management
  • Medical Writing
  • Indian Physicians perspective for Clinical Trials
  • Partnerships in Clinical Trials
  • Pharmacovigilance in India
  • European Pharmacovigilance

    Y K Gupta, National Scientific Co-ordinator,
Pharmacovigilance Programme of India
PK/PD Studies workshop : A one day workshop for biostatisticians to learn the latest advances in Pharmacokinetics/Pharmacodynamics studies



CPhI Conferences India