Regulations
How do you ensure your company is fully compliant on an international level? As one of the most heavily regulated industries in the world, it is pivotal that you stay up to date with the latest legal changes in the pharmaceutical industry. Whether it’s regulation in the EU, United States, Russia, India or anywhere in between, we cover it all through a wide range of resources, including timely news updates, analysis, reports, infographics and videos.
Temperature Controlled Logistics Trends 2023
July 28 by Joanna EdwardsA trends report from Pharma IQ for the pharmaceutical temperature controlled logistics industry, looking at technology, challenges, solutions, and the path to digital transformation.
Overcoming Pharma Supply Chain Obstacles During a Crisis
July 28 by Joanna EdwardsIn conversation with Pharma IQ, Vickram Srivastava delves into the significant challenges the pharma supply chain industry faced during the first two years of the COVID-19 pandemic.
The Regulatory Shift - How Sustainability is Shaping Pharmaceutical Logistics
July 28 by Joanna EdwardsIn this exclusive interview, logistics expert Mark Edwards shares his insights on how the pharmaceutical industry can incorporate sustainable practices into its logistics and supply chain operations.
Mastering the Art of Temperature Controlled Logistics - A Roadmap for Biopharma Companies
July 26 by Joanna EdwardsNavigating temperature control and logistics strategy is critical as pharma and biopharma companies transition from clinical to commercial stages. Pharma IQ's comprehensive guide provides a roadmap fo...
Seven steps to ensure you are GDP-inspection ready
November 18 by Pharma Logistics IQPharma Logistics IQ explains how to maintain standards and mitigate risks with effective GDP compliance.
Bringing IDMP to life for patients: progress in 2019/2020
November 15 by Pharma IQAs IDMP proof-of-concepts start to showcase patient benefits, Frits Stulp calls for increased cooperation and a patient-centric mindset
[Webinar] Everything you need to know about the Russian serialization requirements
November 19 by Pharma LogisticsThis webinar will cover the full scope of the serialization requirements in Russia, including all mandatory labeling requirements for 2019 and 2020
Three reasons to digitally transform Regulatory Affairs
March 14 by Eric Gaussens, PhDErick Gaussens, PhD dissects how stronger information management can transform regulatory affairs
A guideline for EUFMD implementation
October 11 by Pharma Logistics EditorIn Europe, about 1% of medicines, sold to the public through the legal supply chain is fake. To counter the growing threat of counterfeiting, the EU Commission passed the EU Falsified Medicines Direct...
Brexit risk to European medicine supply 'revised down'
September 27 by Pharma Logistics IQ NewsPharmaceutical companies are finding ways to avoid post-Brexit supply issues, according to the European Medicines Agency.
New EU clinical trial guidelines lays down the principles for the two-step release procedure
July 19 by Adam MusprattThe EU published a draft guideline for the responsibilities of sponsors with regard to handling and shipping of investigational medicinal products (IMPs) for human use
Serialization: The US system is not ready for 2019
June 14 by Perry FriThe recent serialization innovation summit from Adents examined how the US’ Drug Supply Chain Security Act compliance is tracking.