Pharma Technology Focus @PharmaTechFocus
A digital magazine bringing you the latest trends and technologies in the industry. With daily news from Pharmaceutical Technology https://t.co/158ZeZ0UND pharma.nridigital.com Joined February 2011-
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RealTime eClinical Solutions' SOMS platform, which is streamlining site operations and accelerating trial timelines, has won this year's Innovation Award. RealTime also won the Marketing award for their strategic rebranding initiative. Read more: tinyurl.com/bdz7pytv
AUTOMA+ 2025 (24-25 November, Vösendorf, Austria) gathers leading companies such as Takeda, Accord Healthcare, Sandoz, Novartis, Bayer AG, Novo Nordisk to explore digital innovative solutions for the pharmaceutical industry. Be a part of the Congress: sh.bgs.group/303
We're pleased to announce our new media partnership with @AAPSComms PharmSci 360, in San Antonio this November. Join us and register today - lnkd.in/ef_qiw_i #PharmSci360
i3 Membrane has been recognized with three prestigious honours at the 2025 Pharmaceutical Technology Excellence Awards, winning in the categories of Innovation, Research & Development, and Environmental. Find out more here - lnkd.in/g-6-tMbX
The London Biotechnology Show 2025 is just around the corner! Meet 3,000+ industry leaders, explore 110+ cutting-edge exhibitors & discover the future of #biotech Visitor Passes are FREE – Register now → tinyurl.com/4vy8fnht #LifeSciences #Pharma #MedTech #HealthTech
TrialWire wins the Innovation Award at the 2025 Clinical Trials Arena Excellence Awards! Honoured for tackling patient enrollment challenges with AI-driven tools, risk-share models & rapid recruitment. Find out more - bit.ly/4dZocgA@
Congratulations to @novotechCRO who have been honoured in the 2025 Pharmaceutical Technology Excellence Awards across three major categories: Diversity, Research and Development, and Marketing. Find out more here - bit.ly/3F0J8Ha
Celebrate 5 years of AUTOMA+! Join pharma leaders and digital experts in Vösendorf, Austria on 24-25 November 2025. Productive networking, various types of sessions, focus exhibition, gala dinner, grand lottery and more! Register: sh.bgs.group/2pn
Visitor Registration is Live! Join the UK’s leading biotech event to explore ground-breaking biotech innovations, connect with global healthcare leaders, and discover the future of life sciences for free. Download your free pass at: tinyurl.com/mw4mzxt6
Alberta partners Siemens and the Alberta Cancer Foundation Siemens Healthineers will contribute $122m to establish two centres of excellence and further research initiatives. pharmaceutical-technology.com/news/alberta-s…
Augustine secures $85m to advance Charcot-Marie-Tooth candidate AGT-100216 will now enter a Phase I/II proof-of-concept clinical trial for CMT disease, with patient enrolment set to begin later this year. pharmaceutical-technology.com/news/augustine…
FDA approves IND application for Everest’s cancer vaccine The company completed subject dosing in an investigator-initiated trial of the vaccine in March 2025. pharmaceutical-technology.com/news/fda-evere…
AstraZeneca to invest $2.5bn in R&D centre in China The new centre will focus on early-stage research and clinical development, supported by data science and AI labs. pharmaceutical-technology.com/news/astrazene…
J&J boosts US operations with $55bn investment J&J is the latest pharma company to announce a major US investment, committing to a $55bn influx in the next four years. pharmaceutical-technology.com/news/jj-boosts…
Alnylam challenges Pfizer and BridgeBio with FDA nod for ATTR-CM drug Amvuttra is now approved in the US to treat both cardiomyopathy and polyneuropathy manifestations of ATTR amyloidosis. pharmaceutical-technology.com/news/alnylam-c…
Mastering compliance and copyright in healthcare and MedComms In the fast-paced world of medical communications, understanding reuse rights and copyright compliance is critical, particularly in today’s ever-evolving technological landscape. pharmaceutical-technology.com/sponsored/mast…
China conditionally approves Hutchmed's Tazverik for follicular lymphoma The approval was based on outcomes from the multicentre, open-label Phase II bridging study in the country. pharmaceutical-technology.com/news/china-hut…
European agencies catch up with speedier regulatory pathways for CGTs in the US Shorter trial authorisation timelines for ATMP trials in the US are an advantage for biotechs, say experts. pharmaceutical-technology.com/features/europ…

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