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Pharma Regulatory 2018 - Conference in Mumbai, Maharashtra, India on March 2018 by Virtue Insight. important dates, call for papers, venue, speakers, abstract submission, research paper, paper submission.
Pharma Regulatory 2018
15th March 2018, Kohinoor Continental Hotel, Mumbai, India
"Understanding recent regulatory developments to explore innovative strategies"
Virtue Insight brings you it’s first Pharma Regulatory 2018, focusing on the clarification and interpretation to the most critical regulatory guidelines faced by the Indian Pharma companies.This unique event will bring key stakeholders gather with the aim of promoting and undertaking to continue work towards a more efficient pharma regulatory system. In the spirit of constructive cooperation, this event brings together representatives from the industry and regulators as well as healthcare professionals. The summit features government and regulatory authorities and expert insights to help you tackle and overcome these regulatory challenges, and to improve the drug and device approval processes for pharmaceutical, biopharmaceutical and medical device companies.
KEY THEMES DISCUSSED:-
Registration, Compliance and Approval, Scientific and regulatory challenges worldwide, Product registration and current regulatory intels, Regional government updates on initiatives, cutting backlogs, current guidelines, Regulatory landscape, Evaluating the regulatory anticipations, opportunities and challenges for biosimilar orphan drugs, Drug approval blockades , Investigating the regulatory surroundings for biosimilars in India, The challenges of the Indian Regulation , Pharmacovigilance Regulations , Deciding better schemes for registering a variation and gaining approval in India, Comprehensive views on OTC product registration, License, Compliance, Safety and Risk Control, Cutting down the backlog of Clinical Trial and Marketing Applications , Regulation analyses , Supply chain, Labelling and Distribution,Standards and cooperative strategies needed
WHO SHOULD ATTEND:-
Specifically designed for pharma, biotech, CRO’s, Government and Regulators, Hospitals/Trial Sites, Technology & Solution Providers and med device professionals responsible for
Regulatory AffairsRegulatory Writing/Medical Writing/Publishing/Information/Submissions, Document and eRecords Management, Business Operations/Processing, Labelling, Clinical Trials Management/Data, Clinical Data, Outsourcing/Clinical Outsourcing/Vendor Management, Product Development, Quality Assurance/Quality Control
CONFERENCE REGISTRATION PROCESS:
Email – Kavitha@virtueinsight.co.in or Tel - +91 44 64998743
Join this one day strategical summit which provides insights on the US, Europe and ROW region which presents the major revenue of the top Indian pharmaceutical companies and explore the regulatory developments and innovative strategies.
For more details and updates please visit website.
firstname.lastname@example.org+91 44 64998743