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 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…
