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AEMPS has provided all the Medical Device regulatory submission requirements related to safety guidelines that are necessary to apply for Medical Device surveillance system

Most Up-to-Date Regulatory Intelligence Database covering 100+ Countries Regulations to get Insights for Faster Regulatory Strategy & Market Approval.

Enables you better understand trial design trends to empower data-driven development and portfolio strategy decisions using insights spanning 750k clinical trials globally.

ANSM is working closely with the poison control centers (CAPTV) and the French Society of Pharmacology and Therapeutics (SFPT) to ensure that both pharmacovigilance (CRPV) and addictovigilance (CEIP-A) networks are mobilized.

Denmark’s medical devices regulatory requirements clearly emphasize the fact of safety. Technology leads to faster development of medical devices but it is essential to ensure that such medical devices can be safely used.

VISTAAR, a provider of Regulatory and Clinical Intelligence solutions with AI driven technology for the life sciences industry, brings enhanced Product Analytics & Label Intelligence modules for Drug & Medical Devices.

Brazil medical devices regulatory requirements are primarily dependent on the level of risk associated with the device. Those with lower risk have a simpler registration process compared to those with a higher level of risk.

Clinical Trials in every country has been faced with a serious challenge in the wake of this pandemic.There are certain set protocols that need to be met while conducting a Clinical Trial, FDA clinical Requirements too are well defined but in this current situation meeting these requirements is next to impossible.

Health Canada strictly mentions that sellers and manufacturers of non-prescription drugs should mention all the details on product labels so that Canadian citizens can make their decisions accordingly.

VISTAAR's AI enabled features work comprehensively to monitor pharma regulatory changes, design regulatory reports enabling you to stay compliant with protocols.

Latest News, Important Updates of Pharma, Biotech, Medical Devices & Diagnostics from Global Regulatory and Health Authorities.

https://www.vistaar.ai/blogs/Importing-Drugs-from-Canada-Made-Easier-by-HHS-Norms

IRT has created its footprint in the field of clinical research and has evolved drastically in such a way that it has bought a major difference in perspective of clinical trials over the decades. It faceted itself into the streams from only randomizing the subject and assigning them to a treatment group to managing the overall supplies required throughout the study through supply management.

Medicine and Healthcare products Regulatory Agency (MHRA) United Kingdom (UK) has put forth its guidance concerning pharmacovigilance process to be undertaken post-transition.

Health Sciences Authority (HSA) Singapore has a set of guidelines that needs to be followed while manufacturing or selling any health related products. Recently HSA has updated its guidelines pertaining to In-vitro Diagnostic (IVD) medical devices.

The current pandemic demands for emergency use authorizations (EUA) so that the necessary medical items can be made available to the public with no further delays.