Articles & Video
The Future of the Global Pharmaceutical Regulatory Affairs Industry
In a new interactive ebook, we take a deep dive into the challenges and trends we may see in pharmaceutical regulatory affairs over the next decade.
Pharma and Medical Device Regulations Content Library: Whitepapers and Reports Collection
Explore our collection of exclusive whitepapers and reports covering the hottest topics in pharma, biotech and medical device regulatory affairs and law with one simple registration.
What is standing in the way of global harmonisation?
Despite many efforts to globalise the pharmaceutical market, why are regulatory affairs still a challenge for drug manufacturers? Figen Kabadas highlights the obstacles.
REPORT: The Future of Healthcare Post COVID-19
In our latest report learn how healthcare organizations are adapting to succeed post COVID-19, from innovation to product development.
Women in Pharma: 44% of pharma professionals think that women are under represented in their organization
44% of pharma professionals think that women are under represented in their organization according to new data from an Informa Connect Life Sciences study. Here we deep dive into the data.
Regulations in Brazil: What the drug approval process is like in 2020
How has Brazil and LATAM adapted pharmaceutical regulations according to COVID-19 and harmonisation with other regions?
SURVEY: Partnering and Deal-Making in Biopharma through the Pandemic
We are conducting a huge study to gauge perspectives around biopharma deal-making during COVID-19 and the commercial ramifications of the pandemic. Take part here.
Barriers and Challenges for Global Regulatory Harmonization
What obstacles are keeping regions such as Latin America from achieving regulatory harmonization with the rest of the world?
Oligonucleotides and peptides: the regulatory challenges
We investigate where current regulatory obstacles lie surrounding peptide and oligonucleotide therapeutics.
Top Biotech Deals in China
Discover the deals transforming China biotech! More than $12 billion in biopharma financing, alliances, IPOs, and new funds have been generated so far this year in China. Learn the details of these deals when you read this new free infographic.
Pharma R&D Annual Review 2020
The researchers and analysts at Pharma Intelligence have taken the guess work out of figuring out how pharmaceutical research and development has progressed over the past few years and what you can expect in 2020. Pharma R&D Annual Review 2020 condenses the thorough analysis of all drugs in development by pharmaceutical companies, from those at the preclinical stage, through the various stages of clinical testing and regulatory approval, and up to and including launch.
80% of life sciences professionals predict a COVID-19 vaccine will be approved within 18 months
How quickly to life sciences professionals predict a COVID-19 vaccine will be approved and what are the main obstacles? We explore.
The EU MDR Delay and Implementation - MedTech eBook Series
Discover the challenges of EU MDR implementation and impacts of the delay on the medical device industry in this MedTech eBook.
The biggest breakthroughs in life sciences the last 10 years
CRISPR, CAR-T, immunotherapies, genome sequencing, AI - what is the biggest breakthrough in the life sciences in the last 10 years?
Brazil & LATAM Pharmaceutical Regulations: Global Harmonisation & the Impact of Covid-19
We speak to two industry experts about how Brazil and LATAM region is working toward global regulatory harmonisation.
Diversity in the life sciences workplace: Implementing a leading corporate culture for innovation - WHITEPAPER
This paper looks at how to foster racial, gender, geographical, neuro and cognitive diversity in the life sciences to achieve an inclusive culture built for innovation.
REPORT: Diversity, Inclusion and Sustainability in the Global Life Sciences Industry 2020
Diversity and Inclusion in Life Sciences 2020: Research analysis of how life sciences professionals around the world view representation of women and minorities in the industry, plus the importance of sustainability.
The Future of IDMP: Quick Fire Questions with the Experts
We spoke to five experts from across regulatory information management about IDMP, the impact of COVID-19 and common obstacles.
Global Pharmaceutical Regulatory Affairs Digital Week offers live practical advice
From future RIM to implementing IDMP, we take a first look at the insightful sessions of the new webinar series coming 24 June.
COVID-19: Advice from the legal experts
We asked legal experts for their best tips and advice for pharmaceutical organisations during the COVID-19 pandemic.
Looking to 2030 Report: The Future of the Global Life Sciences and Pharma Industry
This exclusive report looks at predictions for how the global life sciences and pharma industry will change over the coming decade.