Aaveg Mishra’s Post

🌟 Exciting Panel Announcement! 🌟 Meet Russell, our panel member for MIC's Biggest Conversation! 🎙️ Currently leading at the Medicines and Healthcare products Regulatory Agency (MHRA), Russell spearheads the regulation of Artificial Intelligence as a Medical Device (AIaMD). Get ready for an insightful discussion as Russell shares his wealth of knowledge at MIC's Biggest Conversation! 🗣️ #MICsBiggestConversation #AIinMedicine #PanelSpeaker #AIEvent #Maidstone 🚀

Enjoying day 1 of OCT UK and Ireland. I’m here representing Fisher Clinical Services, talking to sponsors about their plans for clinical trials and how we can support with industry leading clinical packaging and supply services. If you’re here be sure to say hello. #OCT #ClinicalTrials #ClinicalStudies #ClinicalSupply #DrugDevelopment

FDA can be your Partner. In my career, I’ve seen many different approaches of companies to FDA: including confusion, arrogant disregard, and trepidation. However, the key to successful interaction is early engagement and forming a sense of partnership. Why? Because regulators want to bring new therapies to the patient as much as we do, with an eye first on safety, then on efficacy. A perfect example of partnership is a group with which I am quite honored to be affiliated: the CCALC (Cross-Company-Abuse-Liability-Council), which was founded in 2006. One purpose of CCALC is to define best-practice in determining whether a new drug is likely to become a drug of abuse. We continue regularly to meet with FDA, DEA and NIH in order to ensure that we, as an industry, remain at the top of our game. 😊

Speed, Efficiency, and quality. Good people, and processes aligned with client vision = Success

What's the pre-commercial phase look like? It's all about optimizing your plan and team to navigate a successful transition from trials to launch 👉https://rsm.us/40Tu7fq

Psephos’ Irfan Hassan is attending the UK Regulatory Science & Innovation Networks Programme: Collaborative Networking Event today in London. Innovate UK and Innovate UK Business Connect welcome Discovery Phase Regulatory Science & Innovation Networks to come together with stakeholders from all parts of Innovate UK, the Office for Life Sciences, Medicines and Healthcare products Regulatory Agency (MHRA), and the wider regulatory and policy landscape to share best practice and explore options for future collaboration.   We wish you all a successful day and are looking forward to hearing about the potential collaborations. #medtech #medicaldevices #lifesciences #MHRA #regulatorycompliance

We recently hosted the MassMedic Regulatory Roundup, a must-attend event for RA, QA, and C-level executives in the medical device industry. Attendees gained valuable insights on the latest global and domestic regulatory issues affecting the industry. We're proud to support the medical device community and help drive innovation in healthcare. #KPMG #MassMedic #RegulatoryRoundup #MedicalDeviceIndustry #HealthcareInnovation #KPMGBoston

In an era of renewed fiscal responsibility are you doing everything you can to reduce clinical trial costs while maximizing resources?

Are you attending #RAPSConvergence? Stop by booth #300 to meet the Certara team. On October 5, be sure to attend Heather Graham and Trevor Standish’s presentation on "The Evolution of Regulatory Submissions and Technology." Explore how regulatory processes and tech are changing for faster access to medicine. Learn more: https://ow.ly/eomg50PPix4

CROs Maximize Efficiency, Minimize Effort: Explore CTB's revolutionary approach to proposal creation. Spend less time on paperwork, more on winning clinical trials. #EfficiencyUnlocked #CTB #clinicaltrials #clinicalresearch #clinicaltrial #clinicalresearchjobs