Global Bio-Clinical Trials

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Categories: Clinical Biochemical Genetics, Medical

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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

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