Accestra Webinars In collaboration with Pharma To Market, we invite you to join us for a complimentary webinar on 24 October 2024. Mastering Registration of Drug Master File (DMF) in China for APIs, Excipients & Packaging Materials Are you navigating the complexities of Drug Master File (DMF) registration in China? Join us for an exclusive…
Accestra Webinars In collaboration with Pharma To Market, we invite you to join us for a complimentary webinar on 29 October 2024. Pharmacovigilance in China Stay informed on the latest developments in Pharmacovigilance (PV) in China. Join us for this insightful webinar, where industry experts will provide a detailed overview of China’s evolving PV landscape and the…
Time and Location: 07 – 09 May 2024 |Pennsylvania Convention Center, Philadelphia INTRODUCTION CPHI creates connections and inspires partnerships across the global pharma community. Access endless opportunity to grow your business and expand your network at the heart of Pharma! We’re thrilled to announce that our Senior Regulatory Affairs Raymond Ng will take the stage…
Time and Location: 6-8 May 2024 |Berlin Congress Center Alexanderstraße 11, 10178 Berlin, Germany INTRODUCTION RAPS Convergence is the largest and most recognized annual gathering of global regulatory affairs professionals. Convergence brings together representatives of industry, regulatory bodies, research, academia, and clinical organizations that are directly involved in managing the regulatory process and aligning science,…
This Forum provides valuable insights into the most pressing issues QPPVs are facing today. This event has limited capacity, register early! Time and Location: 8 – 9 November 2023 | Amsterdam, Netherlands Meet us in Amsterdam, engage with our speakers face to face about China QPPV requirements and practices, and get real-time feedback for…
Date:19 September 2023 Time:15:00-16:00 (GMT) 10:00-11:00 (ET) 22:00-23:00 (Beijing Time) WEBINAR INTRODUCTION This webinar is about China Drug Master Filing (DMF) comparing with EU and U.S DMF. The presentation provides an overview of the DMF regulatory systems covering Active Pharmaceutical ingredients (API), Excipients & Packaging Materials. Thanks to the global harmonization efforts, the Chinese DMF…
Time and Location: 3 – 5 October 2023 | Palais des Congrès de Montréal 1001 Pl. Jean-Paul-Riopelle Montreal, QC INTRODUCTION RAPS Convergence is the largest and most recognized annual gathering of global regulatory affairs professionals. Convergence brings together representatives of industry, regulatory bodies, research, academia, and clinical organizations that are directly involved in managing the…
Time and Location: 19 – 21 September 2023 | Boston Convention and Exhibition Center INTRODUCTION The largest bioprocessing event for learning how to accelerate promising biologics, cell & gene therapies towards commercial success. Access the science, technologies, and contacts you need to improve efficiencies across all phases of biopharmaceutical development and production. We’re thrilled to…
Time and Location: 24 – 26 October 2023 | Fira Barcelona Gran Via, Spain INTRODUCTION CPHI BioProduction is dedicated to leveraging partnership and collaborations to achieve greater success for production and market access of biologics. We are thrilled to be part of this exciting conference in the vibrant city of Barcelona on 24-26 October. We…
Time and Location: 24 – 26 October 2023 | Barcelona, Spain Meet us in Barcelona, engage with our speakers face to face about China GVP and relevant regulation changes, and get real-time feedback for your questions. INTRODUCTION Pharmacovigilance regulations in China are constantly evolving and rapidly changing. With China becoming increasingly important for pharmaceutical companies,…
Accestra Webinars In collaboration with Pharma To Market, we invite you to join us for a complimentary webinar on 21 June 2023. Pharmacovigilance in China The webinar will cover these topics: Overview of China PV framework Updates on China’s GVP policies Updates on China’s GVP policies Best practices for compliance with China’s GVP requirements and…
Accestra Webinars In collaboration with Pharma To Market, we invite you to join us for a complimentary webinar on 16th May 2023. Drug registration overview in China The webinar will cover these topics: China Drug Regulatory Framework China Drug Registration Overview Imported Drug Registration including overseas data acceptance and regulatory challenge Date : 16 May…
Conference Introduction RAPS Euro Convergence is the most comprehensive regulatory affairs conference in Euro. We are excited to attend the conference in Amsterdam on 10-12 May. This certainly is a valuable opportunity for regulatory affairs professionals worldwide to connect, learn from one another, discuss industry trends & best practices, and expand networks! If you are…
Time and Location: 24 – 25 May 2023 | London, UK Meet us in London, engage with our speaker face to face about China GVP and relevant regulation changes and get real-time feedback for your questions. INTRODUCTION Pharmacovigilance regulations in China are constantly evolving and rapidly changing. With China becoming increasingly important for pharmaceutical companies,…
Accestra Webinars In collaboration with Pharma To Market, we invite you to join us for a complimentary webinar on 17th April 2023. Registration of Drug Master File (DMF) in China for APIs, Excipients & Packaging Materials The China DMF registration webinar will cover these topics: China DMF Regulatory Framework China DMF Pathways Comparison between China…
Click To Download/Read The Full Q&A Content Click To Download The Slides Q1: If have integral DDC product with lots of device (packaging) info in Modules 3.2.P.2.4 & P.7 can you simply x-ref to these sections for safety, tesing/CoA’s, stability etc. A1: Considering the definition of DDC product in China could be different with other…
Q1: If have integral DDC product with lots of device (packaging) info in Modules 3.2.P.2.4 & P.7 can you simply x-ref to these sections for safety, tesing/CoA’s, stability etc. A1: Considering the definition of DDC product in China could be different with other countries, it is crucial to clarify the classification of DDC products in…
ACCESTRA WILL BE PRESENTING AT THE WEBINAR “COMPARISON OF CHINA DMF WITH EU AND US” ON TOPRA. Date: 22 Feb 2023, Wednesday Time: 15:00-16:00 GMT 10:00-11:00 Eastern Time Date: 22 Feb 2023, Wednesday Time: 23:00-24:00 Beijing Time Webinar Introduction This webinar is about China Drug Master Filing (DMF) versus EU and U.S DMF. Accestra will…
Accestra will be presenting at the webinar “China’s OTC Drug Market – Growth Potentials” hosted by the U.S. Commercial Service in China Date and Time: Wednesday, 15th June, 2022, 4:00-5:10PM (Pacific Time), 8:00-9:10PM (Eastern Time) Thursday, 16th June, 2022, 8:00-9:10AM (Beijing Time) COST: USD25 per participant Click here to register. You will then receive an…
Topic: China Drug Master File (DMF) Filing Agenda: Regulatory Framework & Registration Comparison among China, EU & US Common Challenges Questions and Answers Date and Time: 25th May (wed) 5:00-6:00 pm China time Time: Jun 9, 2022 10:30 AM in Paris Speakers
What’s new for Good Pharmacovigilance Practices (GVP) in China In collaboration with Pharma to Market, join us for a series of two complimentary webinars as we give you an introduction into the latest policy updates on the Good Pharmacovigilance Practices (GVP) in China, Singapore & Malaysia in the final week of May 2022. What’s new…
In collaboration with Accestra Consulting. we invite you to join us for a series of four complimentary webinars in the first 2 weeks of April 2022. Introduction to Generic Drug Registration in Malaysia, Singapore, Vietnam and ChinaThe generic drug registration webinars will cover these topics for each country: Regulatory Framework and Pathways Registration process and…
A Whole New Game? Innovation and Regulation in China and Switzerland Switzerland is home to a highly innovative life sciences cluster. Many multinational corporations, as well as a network of smaller companies and startups have operations in Switzerland, mostly in the Basel Area. The industry is vibrant, with many innovative developments occurring in pharmaceuticals, biotech…
Mandatory GACC registration for all F&B exporters from 1 January 2022 On 8 December 2021, the EU SME Centre and its leading consortium partner, the China-Italy Chamber of Commerce, held their webinar on new major regulations from the General Administration of Customs of China, which require all overseas F&B manufacturers exporting to China to have…
Date: Wednesday, 8th December, 2021 Time: 4 – 5:30 (Beijing） Time: 9 – 10:30 AM CST (Brussels) Price: Free of charge Click here to register. You will then receive an invitation to this webinar. Please note that the number of participants is limited. TOPICS and SPEAKERS: In April 2021, China’s General Administration of Customs (GAC)…
Date: Tuesday, 9th March, 2021 Time: 7:30 AM – 8:30 AM CST (China Standard Time) Price: Free of charge Click here to register. You will then receive an invitation to this webinar. Please note that the number of participants is limited. TOPICS and SPEAKERS: Pete Frost: Trade Commissioner, Greater China, New Zealand Trade & Enterprise…
Join free webinar on China Drug Master File (DMF) Filing for APIs, Excipients & Packaging Materials (click here to register) on Thursday 15th April, 2021, at 10:30 CEST time. The webinar will provide an overview of the requirements, regulatory pathways, how to register your DMF in China and a comparison between US FDA and EMA…
Tuesday 2 June, 1.30 – 2.30pm (NZST) Brought to you by New Zealand Trade and Enterprise (NZTE), this webinar series has been designed to help your business navigate the shifting digital landscape in post-COVID China. From mastering your digital strategy and optimising your social media investment, to understanding consumer behaviour and regulatory considerations/compliance, our experts…
Due to the US-China trade war, American delegates at Shanghai’s SIAL Food Expo decreased by 50% this year. No wonder China’s market has become more difficult for US firms when, for example, US wine tariffs are 70% (no FTA and trade war tariffs) while Australia’s are 0% (ChAFTA). On the latest Australia China Business Council…
Date: Tuesday, 12th May, 2020 Time: 13:30-14:30 CST (China Standard Time) Price: Free of charge Brought to you by New Zealand Trade and Enterprise (NZTE), this webinar series has been designed to help your business navigate the shifting digital landscape in post-COVID China. From mastering your digital strategy and optimising your social media investment, to…
