The world's leading automated proofreading software
Levelling Up in the Medical Device Submission Game
Sept 23, 2024
This is a rare opportunity to meet with the FDA, Health Canada and MedTech Canada all at once. The workshop will focus on demonstrating the value of recognized and consensus standards, explain how to cite them to maximize efficiencies, including in eSTAR, and introduce participants to FDA’s latest program to enhance standards’ use: the Accreditation Scheme for Conformity Assessment, or ASCA.
TOPRA Symposium 2024
Sept 30 – Oct 2, 2024
This year’s TOPRA Symposium takes place in Rotterdam, the Netherlands, on 30 September – 2 October 2024 and is being held in partnership with the Medicines Evaluation Board (MEB), the Netherlands’ national authority of medicines and health products.
RAPS Convergence 2024
Sept 17-19, 2024
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, regulation, and business strategy.
EskoWorld 2024
June 25-27, 2024
Schlafender Hase is a proud Gold Level Sponsor of EskoWorld 2024. The 33nd annual event, gathering Esko users from around the globe for an exciting and informative series of discussions exploring accomplishments, shared obstacles, and industry trends and best practices.
4th Annual Pharmaceutical Regulatory Affairs Summit
May 15-16, 2024
The 4th Annual Pharmaceutical Regulatory Affairs Summit has been meticulously crafted to comprehensively address the pressing issues in Regulatory Affairs, including the transformative impact of digitalization and AI. In addition, our event will spotlight the following hot themes: patient-centeredness, fostering innovation, and navigating the ‘adjustments to EU Pharmaceutical Strategy’ and many others.
RAPS Euro Convergence
May 6-8, 2024
RAPS Euro Convergence is the most comprehensive regulatory affairs conference in Europe, focusing on the latest developments in healthcare products in Europe and beyond—medical devices, IVDs, pharmaceuticals, and AI and Software.
GCC Regulatory Affairs Pharma Summit
April 22-23, 2024
GCC Regulatory Affairs Pharma Summit is an annual event that provides platform for pharmaceutical regulatory experts and industry professionals in the GCC region to share insights and discuss about the latest updates in the pharmaceutical regulations.
Global Labeling
March 14-15, 2024
DIA’s Global Labeling Conference is designed for professionals in medical product labeling and related disciplines as they work to develop and manage clear and accurate labeling information for the safe and effective use of prescription drugs, biologics, and medical devices.
Advertising and Promotion Regulatory Affairs Conference
March 12-13, 2024
DIA’s Advertising and Promotion Regulatory Affairs Conference is in its 35th year! The conference explores the current state of compliance for marketing both biopharmaceuticals and medical devices.
Regulatory Submissions, Information & Document Management Forum
February 12-14, 2024
At DIA’s Regulatory Submissions, Information, and Document Management (RSIDM) Forum, we will hear from industry and regulatory stakeholders working across the scope of regulatory information to examine current and evolving data standards and requirements and effective regulatory information management approaches to align related people, processes, and technology.
MedTechLabelling
November 22-23, 2023
The 3rd Annual European Medical Device and Diagnostic Regulatory Affairs Conference is the most comprehensive conference focusing on the latest regulatory development and challenges in healthcare products in Europe and beyond.
TOPRA Symposium
October 23-25, 2023
Held annually since 2004, the TOPRA Symposium is Europe’s premier conference for healthcare regulatory affairs. With dedicated programme streams for human medicines, medical devices and IVDs, and veterinary medicines, the Symposium is the must-attend event in the regulatory affairs calendar.
Precision in Medical Devices Summit
October 16-17, 2023
Join us at the 21st Precision In Clinical Trials Summit (San Diego). The PCT USA West Coast Summit for a two-day journey into the insightful world of clinical trials. You’ll connect with an incredible gathering of experts and uncover practical advice from industry-leading researchers, peers, and executives.
Pharma Packaging Labeling and Device Innovation Forum
October 5-6, 2023
9th Pharma Packaging and Labeling Innovation Forum 2023 is an executive platform to discuss the industry challenges for Material & Design Innovations, Sustainability, Branding & Marketing, and Inspirational & Active Packaging.
RAPS CONVERGENCE 2023
October 3-5, 2023
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, regulation, and business strategy.
EskoWorld 2023
May 23-25, 2023
Schlafender Hase is a proud Gold Level Sponsor of EskoWorld 2023. The 32nd annual event, gathering Esko users from around the globe for an exciting and informative series of discussions exploring accomplishments, shared obstacles, and industry trends and best practices.
2023 Euro Convergence
Conference: May 10-12th, 2023
Meet the Rabbit at booth 3! RAPS Euro Convergence is the premier annual event where medical device, IVDR, and pharmaceutical regulatory professionals convene to learn, network, and share best practices that foster excellence—personally and professionally.
Precision in Clinical Trials Summit Boston
Summit: May 1- 2, 2023
Join us at 20th PCT Boston Clinical Trials Summit for a two-day journey into the insightful world of clinical trials.
DIA’s Advertising and Promotion Regulatory Affairs Conference
Conference: February 23-24, 2023
Join us at DIA’s Advertising and Promotion Regulatory Affairs Conference. Sessions will explore the current state of compliance for marketing both biopharmaceuticals and medical devices. Join thought leaders from industry, legal, public affairs, and government for interactive and compelling discussions that will shape policy and define strategic priorities within the advertising and promotion regulatory space.
