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International Pharma Regulatory Summit 2017

Date: 27th July 2017 - 28th July 2017 Location: Singapore

Effectively interpret complicated regulatory guidelines to fast track your drug approval process

Asia’s regulatory systems are diverse, and oftentimes challenging to navigate. The regulatory agency in each Asian country has its own set of regulations and customary manner of conducting business. Thus, determining the most effective and efficient strategy to obtain approval for your pharmaceutical product from each regulatory body without sufficient knowledge and experience with Asian regulatory affairs can be a very difficult task.

Against this backdrop, ACI brings you International Pharma Regulatory Summit 2017 will enable you to make confident, actionable decisions.

Highlighted features at 2-day conference includes

  • Regulatory submissions implementation in eCTD format
  • The ASEAN Labelling Harmonisation Effort
  • Registration and approval timeline – combination products and exemptions
  • What’s new with clinical regulatory requirements in Asia Pacific?
  • Global trends vs. specific region’s updates for pharmacovigilance
  • Regulatory affairs support in providing advices to commercial team for inspection
  • Global Guidelines for the Development of Biologics


International Pharma Regulatory Summit 2017 - Conference Pass (Inc. Documentation Package)£1,275.00Inclusive of £320 early bird discount, valid till 31st March 2017
International Pharma Regulatory Summit 2017 - Documentation Package Only£420.00


27th July 2017
28th July 2017
Event Category:


Oby George – Content
+91 (0) 20 6527 2804
Priyesh Waghmare – Marketing, Sales & Media Partnerships
+91 (0) 20 6527 2803
Vivek Hankare – Sponsorship
+91 20 6527 2803
Claire Taylor-Payne – Logistics
+ 44 (0)20 3141 0601


We will confirm the venue approximately 4-6 weeks before the event to ensure we find the most suitable space because numbers can vary dramatically. There will be a discounted accommodation rate for conference attendees.
Singapore, Singapore
+ Google Map

Directors/Heads/Managers of Regulatory Affairs, Quality Control, Quality Assurance, Patent/Intellectual Property Rights /Legal, Pharmacovigilance/Drug Safety

Confirmed Speakers

  • May Ng, Regulatory And Quality Consultant,Founder, ARQon
  • Widyaretna Buenastuti, Public Affairs & Communications Director, Pfizer Indonesia
  • Shibu Baburaj, Head, Regulatory Affairs/ CMC, Sanofi-Aventis

If you would like to be considered as a speaker for the event with a 20-35 minute presentation, please submit an abstract along with your bio to:

Oby George

Tel: +91 (0)20 4120 0839

email: ogeorge@acieu.net  

ACI has put together a range of packages to suit your requirements. These range from branding options, to full scale partner solutions and can be tailored to meet your objectives and budgets.

If you are launching a new product or service and wish to gain visibility and brand recognition within your industry, contact us today!

For commercial opportunities, please contact:

Vivek Hankare

Tel: + 91 (0) 20 6527 2804

Email: vhankare@acieu.net