2nd Annual Pharma Regulatory Summit 2019

On Jan 21, 2019

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.