Partnered Content
Pharma Ignite (Citeline’s marketing insights division), brings together a network of 400+ industry analysts, editors, marketers, and our clients to deliver fresh content, insights and establish connections between clients and pharma’s leaders.
Armed with Citeline’s subscribers and solutions including Scrip, Pink Sheet, In Vivo, Generics Bulletin and Medtech Insights, leverage our industry knowledge to build brand credibility, generate leads and create thought leadership and engaging content.
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Latest Articles
Learn how advances in vaccine adjuvants are shaping the future of global health and driving more effective immunization strategies

Learn more about the challenges faced by today’s drug developers and the critical factors to consider as sponsors navigate the supply chain, keep up with regulatory requirements, and ensure patient access. Discover more about the role of generics and how Aspire Pharma can help.

Delve into the challenges facing the NHS, from rising medicine costs to supply shortages, and how generics and branded generics can provide solutions for a more sustainable healthcare system
Learn about the critical role the right CRO plays in successfully navigating the significant drug development opportunities in Japan.
Research Reports
Cell and gene therapy sponsors are increasingly faced with hard decisions focused around mitigating potential delays.
Blending Human Experts With AI Agents Cuts Costs, Increases Access, And Improves Customer Experience
Almost 50% of biopharma are con-sidering China for clinical studies because of vast patient pools, competitive approval pathways, and cost savings.
Oncology continues to lead the way as a therapeutic focus for the pharma industry.
Roundtable Reports
CGTs are among the fastest-growing areas in therapeutics - explore the key strategies driving long-term commercial success across the entire product lifecycle.
Access key takeaways from a roundtable on the evolving landscape for rAAV-based gene therapies. Experts discussed approaches to clinical development, regulatory barriers, and the future outlook for AAV developers and lab services organizations.
Overcoming Immunogenicity And Safety Assessment Challenges For Biologics And Biosimilars In Oncology
Expert panelists discuss regulatory challenges, flexible approaches to assay selection, and applying scientific reasoning with guidelines to address immunogenicity and safety assessment challenges in oncology biologics and biosimilars.
Stay current with trends in infectious disease clinical trials, with fresh insights from a recent roundtable event. Discover how the landscape is evolving and what to expect in the future, with key takeaways from industry experts.
Webinars
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Speed, security, success: Innovations in cold chain packaging and labeling for clinical trials
In partnership with Thermo Fisher Scientific
- Industry Outlook: Benchmarking Biopharma’s Next Wave of Clinical Data Transformation
In partnership with eClinical Solutions
- Stop outsourcing, start partnering: Redefining value in global clinical trial execution
In partnership with Thermo Fisher Scientific
- Beyond development: Using continuous manufacturing to accelerate OSD commercialization
In partnership with Thermo Fisher Scientific
- De-Risking Development with Specialized Data Strategies - From Trial Design to Submission
In partnership with MMS Holdings
- Delivering Value in Clinical Trial Logistics: Managing Complexity, Accelerating Timelines, and Embracing Innovation
In partnership with Thermo Fisher Scientific
- Clinical Ancillary Management: Reducing Risk And Improving Readiness In Global Trials
In partnership with Thermo Fisher Scientific
- Revolutionizing Gene Therapy Manufacturing: Robotics And Machine Learning For Process Intensificiation
In partnership with Thermo Fisher Scientific
- Enhancing Aseptic Fill Finish Processes with Advanced Solutions
In partnership with Thermo Fisher Scientific
- Accelerating Scientific Innovation: Scalable, Turnkey Lab Solutions for a Global Market
In partnership with SmartLabs
- Unlocking the Potential of Target Product Profiles (TPPs) in Modern R&D: Exclusive Insights from a New Industry Survey
In partnership with IQVIA
- What’s really happening with GLP-1s? What real-world data tells us.
In partnership with Truveta
- Innovative Approaches to Clinical Trial Financial Management
In partnership with IQVIA Technologies
- From model to molecule: Combining AI and experimental strategies to transform drug development
In partnership with Thermo Fisher Scientific
- Future-Ready Pharmacovigilance: Integrating AI With FDA's EDSTP Guidelines
In partnership with IQVIA
- Accelerating Biologics Development With Strategies For Success
In partnership with Thermo Fisher
- Securing your samples: Strategies for safeguarding critical biological materials
In partnership with Thermo Fisher
- qPCR and dPCR Technologies as Complementary Tools in the Development of Cell and Gene Therapies
In partnership with Thermo Fisher
- Enhancing Pharmacovigilance Intake Processes With AI And Automation
In partnership with IQVIA
- Maximizing value across drug development: Embracing a new CDMO and CRO partnership approach
In partnership with Thermo Fisher
- Safety & Regulatory Compliance Predictions For 2025: Unlock Future Trends With IQVIA
In partnership with IQVIA
- Unlocking the Potential: Challenges and Opportunities in Oral Delivery of Peptides
In partnership with ThermoFisher
- Getting the Most Out of Your Lab Space: Design & Operational Considerations
In partnership with SmartLabs
- Fast Track Your Path To Commercialization:
Maximize Scale-Up For Efficiencies In Process Development
In partnership with ThermoFisher
- Generative AI in Literature Extraction: Boosting Efficiency In Pharmacovigilance
In partnership with IQVIA Technologies
Webinar Executive Summaries
Computer systems validation (CSV) has long been a regulatory necessity but is considered time and resource-consuming to execute.
In recent years, global regulatory requirements have evolved in many areas of the MedTech product life cycle management.
Despite widespread recognition of the importance of diversity in clinical trials, most trials still fail to recruit diverse participants.
Fourier-transform infrared (FTIR) spectroscopy is one of the most common forms of infrared spectroscopy and one of the most popular analytical techniques for quality assurance (QA), quality control (QC), and materials identification in the pharmaceutical industry.
eBooks
Discover how transforming field reps from “Wild Cards” to “Masters of the Message” in Pharma Omnichannel Marketing, enhances performance and mitigates risk.
Discover what’s on the horizon for the pharma industry as truly transformative technologies revolutionize the way drugs are developed, delivered and manufactured.
With the pharmaceutical industry still adjusting to the potential impacts of Humira's loss of exclusivity, another milestone for biosimilars has been achieved in 2022.
As we enter the third year of the COVID-19 pandemic, the pharma industry has begun to adapt and grow around its constraints and opportunities.
White Papers
Learn more about how China’s biopharmas are going global by working with dependable and trustworthy companion diagnostics partners.
Cell and gene therapies (CGTs) are continuing to gain momentum in life sciences globally.
Catalytic hydrogenation is a proven green manufacturing process that can transform the synthesis of active pharmaceutical ingredients (API), driving down costs while reducing environmental impact.
The use of mRNA in modern therapeutics is growing in popularity and efficacy.
Infographics

Gain exclusive insights into the biggest challenges biotechs face in oncology and uncover the latest opportunities to accelerate drug development.
Hematological oncology is a growing area of the global pharmaceutical pipeline, meaning more treatments in research and development are set to reach Phase I and II clinical studies.
With delays currently facing drug developers due to some contract manufacturing organizations (CMOs) experiencing backlogs, future expectations for these service providers are being redefined.
Podcasts
Insights from Novotech on Evolving Trends Impacting Global Clinical Development
Discover the latest trends in RNA-based therapeutics and learn how sponsors can successfully navigate the road to next generation innovation. Listen in as Citeline chats with the Director of Therapeutics at Novotech, a CRO experienced in RNA development.
Insights from Novotech on Evolving Trends Impacting Global Clinical Development
Join Andrew Warmington, Manufacturing Editor at Citeline, in conversation with Tom Hickey, Director of Therapeutic Strategy at Novotech, a global full-service clinical CRO dedicated to accelerating the development of advanced and novel therapeutics.
Videos

Lonza is addressing the growing global demand for biologics by utilizing its expert teams and the advanced capabilities of its newly acquired large-scale manufacturing site in Vacaville, California. Joanna McCafferty, Director of Commercial Development, shares more in this brief video. Ask ChatG

Biotechs focus on novel cancer therapies to address the rising global burden. Yet, oncology R&D poses unique, complex challenges. Overcoming these while adapting to an evolving landscape is key to transforming patient care and improving outcomes.
Awards
11 September 2025
London Hilton on Park Lane
21 October 2025
Palace Hotel Tokyo
29 October 2025
Radisson Blu Frankfurt
20 November 2025
Royal Lancaster Hotel
11 December 2025
London Hilton on Park Lane
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