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Pharmaceutical Industry Events this Autumn
We’re at a number of events between now and the end of November, demonstrating our clinical data expertise. Get in touch if you’d like a meeting.
Global Harmonisation of Clinical Trials
Global Harmonisation of Clinical Trials is the latest focus for our quarterly roundup of the regulatory landscape with news from EMA, FDA and ICH
Protocol writing is changing – Estimands (ICH E9(R1))
This month Darren Jolliffe, explains how S-cubed can assist you in applying the forthcoming regulatory guidance ICH E9(R1)
CDISC 360 Project and the A3 Suite
The CDISC 360 Project is a major change in the way we access and use standards. Our A3 Suite is ready and tuned to the vision.
CDISC, PhUSE, DADM – Events Update
It’s been a busy few months for S-cubed. Find out where we’ve been and where we’re going to next.
Statistics and Machine Learning – Cause for concern or excitement?
Statistics and the impact of machine learning get Elizabeth Merrall thinking and considering the future.
Latest News in Clinical Development Practices and Regulations
Our latest Industry Insights focuses on Brexit and news from the regulators around the globe.
10 Years of S-cubed at CDISC: The Interchange 2019
As we head to the CDISC Interchange this week, make sure you see our presentations and meet our team at Stand 11.
S-cubed Announces A3 Informatics Merger and New Partners
S-cubed is pleased to announce that S-cubed and A3 Informatics have merged to bring the A3 Suite of tools inside the S-cubed brand.
Celebrating 10 Years of Regulatory Affairs and Quality Assurance
Regulatory Affairs and Quality Assurance – S-cubed Ltd are 10 years old. Find out about how our team came together and continue to grow.
Data Silos, Demos, Discussions at PhUSE
The latest papers and presentations from PhUSE US Connect in Baltimore and our future events, including CDISC.
Brexit, EMA, FDA & Global Regulatory News
Our first Industry Insights of 2019 focuses on the latest regulatory developments and Brexit.
PhUSE Keynote – A Cautionary Tale
A fascinating talk by the Keynote Speaker, Dr Ahadpour from the FDA on the opioid addiction crisis in the USA.
Regulatory Affairs & Quality Assurance: Copenhagen
Jakob Sandersen reports on the exciting developments at Pharmaceutical Services ApS over the last 15 months.
PhUSE US Connect & CDISC
Learn all about our presentations at PhUSE US Connect in Baltimore and at the CDISC Interchange in Amsterdam
SME Day at EMA – Part 3
The final report on the SME Day at EMA focuses on the Committee for Advanced Therapies, new Medical Devices Regulation and a Brexit update.
Qlik Specialization Status Awarded to S-cubed
Our Qlik Team are proud to announce that they have been awarded Pharmaceutical and Biotech Specialization status.
SME Day at the EMA – Part Two
Part Two of the report from the SME Day at the EMA focuses on Marketing Authorisations and more.
SME Day at the EMA – Part One
Larissa Gould reports from the EMA in Canary Wharf on the latest developments.
Brexit Update, Clinical Trial Data Sharing, & more
Our latest industry update covers news about Brexit, from FDA, EMA and more.
Qlik Team on Tour – Are you part of the Data Revolution?
Our Qlik Team are on Tour in Stockholm. Be part of the Data Revolution and join them there!
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INDUSTRY INSIGHTS
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The industry insights features the latest news and developments from the pharmaceutical industry.
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Featured in this issue of Industry Insights:
- COVID – 19 Guidance Updates
- Clinical Trial Regulation (CTR) EU No 536/2014
- Brexit
- Publishing Trial Results
If you want to contribute or share something that you’d like to be listed in the next issue, please feel free to contact us.