Pharma Regulatory Summit is the leading platform for regulatory experts, to be updated with latest country updates and strategies to navigate the complex and ever changing regulations in the region. This conference will focus on the new strategies, amendments, innovations, developments in the fields of regulatory affairs, intellectual property and medical devices, which reflects new strategies in the field of regulatory affairs. Regulatory Affairs additionally have certain significance inside the Healthcare industries, such as pharmaceuticals, medical devices, biologics and practical nourishments.
SPONSORS:
- Exhibitor: Nishith Desai Associates
KEY SPEAKERS:
- RAMKISHAN, Deputy Drugs Controller, DDC(I), CDSCO
- KALAISELVAN, Principal Scientific Officer, Indian Pharmacopoeia Commission
- KIRAN MARTHAK, Directors – Management, (Vice Chairman of the Medical Committee, IDMA), Lambda
- MAYUR PARMAR, Deputy Collector, Government Of Gujarat
- SHIRAZ KANDAWALLA, Associate Director – Regulatory Affairs,Abbott
- SHANTANU MUKHERJEE, Legal Head, Asia Pacific and Japan, Lupin
- OMPRAKASH S. SADHWANI, Former Joint Commissioner and controlling Authority, Food and Drug Administration (Maharashtra state)
- KEDAR SUVARNAPATHAKI, Head – Regulatory Affairs & IP, Boehringer Ingelheim
- AMITA BHAVE, Head Regulatory Affairs GDD India, Novartis
- SONIKA SHAH, Regulatory Affairs Head, Amgen
- RAJESH NAIK, Head Medical Affairs Oncology, Boehringer Ingelheim
- MILIND ANTANI, Leader, Pharma and Healthcare, Nishith Desai Associates
- ALAP GANDHI, Head, Medical Affairs, GSK
- RITU JOHARI, Head-Scientific Affairs, Quality & Regulatory, Abbott Diabetes Care
- MILIND NARVEKAR, Head Regulatory Affairs, Apotex Research
- R.SALUNKHE, Former Assistant commissioner, FDA Maharashtra
- PRATIK SHAH, (Former Head – Clinical, Medical & Regulatory Affairs, PV and QA Astellas Pharma), Independent Consultant
- VIJAYA ANAND, Chief Manager – Corporate Regulatory Affairs, Piramal
- NISHA FERNANDES, Manager – Regulatory Affairs, Amgen
- HITENDRA BHATIA, Independent Consultant – Regulatory Affairs
WHO SHOULD ATTEND:
This conference is specifically designed for pharma, biotech, CRO’s, Government and Regulators, Hospitals/Trial Sites, Technology & Solution Providers and med device professionals responsible for
Regulatory Affairs, Regulatory 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 SPONSORSHIP:
E-mail – kavitha@virtueinsight.co.in Tel: +9144 24762472
Sponsor, Exhibition Stall (Booth) and a paid Speaker Slots are also available
We also have some sponsorship opportunities available for the event, which gives you an opportunity to sponsor/speak/exhibit, and create brand awareness. In addition, the networking opportunities in focused and relevant industry gathering provide the personal contact necessary for business development efforts.
CONFERENCE REGISTRATION PROCESS:
E-mail – kavitha@virtueinsight.co.in Tel: +9144 24762472
- Early Bird Discount Price (Ends 28th January 2019) – (INR 10,000 + GST (18%) per delegate)
- Standard Price (From 29th January 2019 Onwards) – (INR 15,000 + GST (18%) per delegate)
In order to register you can simply e-mail me your invoice details in the below mentioned format;
- Name:
- Company Name & Address:
- GST Number:
- Job Position:
- Contact Number:
Get more from the event, with a broader scope bringing the whole communications value chain together. Enjoy and make the best out of our dedicated networking drinks time, meet the leading international vendors showcasing the products of tomorrow in the co-located exhibition. Expand your knowledge of the latest business models and strategies in the high-level conference.
https://www.virtueinsight.com/pharma/2nd-Annual-Pharma-Regulatory-Summit-2019/
