Latest in Pharmaceutical

Hanmi licenses UCN2 obesity drug candidate HM17321 to Genentech in $2.3bn deal

Hanmi Pharm has granted Genentech global rights to develop and commercialise HM17321, an investigational UCN2 analogue designed to drive weight loss while preserving lean mass

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Hanmi licenses UCN2 obesity drug candidate HM17321 to Genentech in $2.3bn deal

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Why poor data quality has the potential to derail AI in pharma

Why poor data quality has the potential to derail AI in pharma

Artificial intelligence is rapidly transitioning from a technology pipedream to an operational reality for many businesses in the pharmaceutical and medical device...
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Irish manufacturer brings EU GMP-certified dronabinol API to UK specials market

Irish manufacturer brings EU GMP-certified dronabinol API to UK specials market

Dunbar Pharmaceuticals partners with IPS Pharma to supply plant-derived dronabinol API for UK Specials-pathway cannabis medicines, following its earlier expansion into Germany
Henlius and Sandoz expand global biosimilars partnership with up to ten assets

Henlius and Sandoz expand global biosimilars partnership with up to ten assets

Shanghai Henlius and Sandoz have expanded their existing partnership to cover up to ten monoclonal antibody and antibody-drug conjugate biosimilars, with an initial deal potentially worth up to $322m
Panthera opens clinical research site at Keele University

Panthera opens clinical research site at Keele University

Panthera has opened a new clinical trial site at Keele University, expanding its UK and European research network to 11 locations and increasing access to clinical studies in Staffordshire
Androlabs appoints EffRx as Swiss commercial partner for testosterone therapy Testavan

Androlabs appoints EffRx as Swiss commercial partner for testosterone therapy Testavan

The agreement expands Testavan's European commercial footprint, giving EffRx distribution rights in Switzerland as Androlabs targets an underdiagnosed hypogonadism market affecting an estimated 10-40% of men globally
AstronauTx secures rights to Saniona neurological drug candidate

AstronauTx secures rights to Saniona neurological drug candidate

The firm has exercised its option to acquire worldwide rights to ATX0926 from Saniona, moving the sleep biology-focused small molecule into IND-enabling development
European consortium validates continuous API manufacturing platform

European consortium validates continuous API manufacturing platform

PIPAC combines continuous-flow chemistry, real-time analytics and AI process control to support more flexible and resilient pharmaceutical ingredient manufacturing
OGT begins full IVDR transition for CytoCell FISH probe portfolio

OGT begins full IVDR transition for CytoCell FISH probe portfolio

OGT has launched two IVDR-certified prenatal FISH probe kits as it begins transitioning its full CytoCell portfolio ahead of the EU’s 2028 Class C deadline
Safety in pharmaceutical manufacturing: why a trusted partner makes all the difference

Safety in pharmaceutical manufacturing: why a trusted partner makes all the difference

By taking a three-tiered approach to protecting patients and personnel and ensuring plant compliance, GEA adopts a consultative approach to helping its customers navigate the responsibilities of pharmaceutical manufacturing safety with confidence

Latest posts in Pharmaceutical

CellCarta adds Tempus to companion diagnostic commercialisation network

CellCarta adds Tempus to companion diagnostic commercialisation network

CellCarta has partnered with Tempus to expand its CDx Commercialization Lab Network, giving biopharma sponsors a route from companion diagnostic development and regulatory approval to commercial testing in US oncology practice
Reconstitutable powder filling system for global MedTech client

Reconstitutable powder filling system for global MedTech client

3P innovation's custom automation expertise enables customers to advance product and process innovation across diverse industries
Early phase analytical strategy for biosimilars in a shifting regulatory landscape

Early phase analytical strategy for biosimilars in a shifting regulatory landscape

As FDA and EMA guidance continues to reinforce analytical comparability as the foundation of biosimilar development, investing in comprehensive early-stage characterisation is becoming essential to reduce uncertainty and improve development outcomes, says Dr Andrew J. Reason, CEO at BioPharmaSpec
Alzheimer’s Association launches $100m trial combining lifestyle changes and GLP-1s to prevent cognitive decline

Alzheimer’s Association launches $100m trial combining lifestyle changes and GLP-1s to prevent cognitive decline

The global study builds on US POINTER trial findings, testing whether adding a metabolism-targeting drug to structured lifestyle programmes can further reduce cognitive decline risk in at-risk older adults during a three-year period
Teva and Polpharma Biologics sign global licensing deal for Ocrevus biosimilar candidate

Teva and Polpharma Biologics sign global licensing deal for Ocrevus biosimilar candidate

The agreement will expand Teva’s biosimilars pipeline, with the company securing exclusive commercialisation rights for Polpharma Biologics’ proposed ocrelizumab biosimilar across key global markets
Sanofi offers EU commitments for flu vaccine disparagement claims

Sanofi offers EU commitments for flu vaccine disparagement claims

Sanofi has proposed remedies to EU antitrust regulators after allegations it disparaged rival CSL Seqirus's Fluad vaccine in Germany and France since 2024
IMCD opens new Pharmaceutical Technical Centre in New Jersey

IMCD opens new Pharmaceutical Technical Centre in New Jersey

IMCD has launched a new Pharmaceutical Technical Centre in Allendale, New Jersey, offering advanced formulation support for solid, semi-solid and liquid dosage forms, alongside a co-located Food & Nutrition US Technical Hub
MSD partners with Abu Dhabi to explore regional pharma logistics hub in HELM Cluster

MSD partners with Abu Dhabi to explore regional pharma logistics hub in HELM Cluster

The collaboration would strengthen supply chain resilience and accelerate access to innovative therapies across the region, subject to approvals, positioning Abu Dhabi as a secure distribution gateway for global pharma
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Neuland Laboratories announces new $20m process development lab in Hyderabad

Neuland Laboratories announces new $20m process development lab in Hyderabad

The new facility will be fully operational by October 2026 and will give clients earlier manufacturability insight when looking to scale up, through the incorporation of non-GMP kilo labs as well as AI-driven route scouting, parallel synthesis and ELNs
FDA approves Utebzi, first oral carbapenem antibiotic, for complicated UTIs

FDA approves Utebzi, first oral carbapenem antibiotic, for complicated UTIs

GSK and Spero Therapeutics' tebipenem pivoxil matches IV imipenem-cilastatin in Phase III trials, offering an outpatient alternative for resistant infections that cost the US healthcare system more than $6bn annually
Why Pharma's supply chain technology investments are falling short of resilience

Why Pharma's supply chain technology investments are falling short of resilience

The pharmaceutical industry has spent the best part of six years reassessing its supply chain

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Codis brings together formulation development, spray drying and commercial supply

Codis brings together formulation development, spray drying and commercial supply

Combining expertise across the UK and US, Codis supports customers from material characterisation and formulation development through scale-up, clinical studies and...
Why NSF QP Alumni continue learning, connecting and growing together

Why NSF QP Alumni continue learning, connecting and growing together

Discover why NSF QP Alumni return to continue learning, exchange experience and build trusted relationships that support their professional development and complex...
The foundations of pharmaceutical compliance every new professional needs

The foundations of pharmaceutical compliance every new professional needs

Discover the essential principles of pharmaceutical quality and compliance, and learn why building strong foundations early helps improve performance, support regulatory...
Why high-quality QP training is critical for patient safety and compliance

Why high-quality QP training is critical for patient safety and compliance

Discover why high-quality Qualified Person training goes beyond theory, combining expert mentoring, practical experience and rigorous preparation to support patient safety...
CPHI Milan releases 2026 conference programme, with new Sustainability Summit

CPHI Milan releases 2026 conference programme, with new Sustainability Summit

The tradeshow's October programme features Eli Lilly, BMS and AstraZeneca leaders alongside a new summit on sustainable pharma manufacturing
Designing the future of pharma packaging – in Europe

Designing the future of pharma packaging – in Europe

Are you thinking about sustainable pharmaceutical packaging? ACG is committed to advancing sustainability in pharmaceutical packaging
Formulation freedom in clinical development: Why Fill2Weight matters

Formulation freedom in clinical development: Why Fill2Weight matters

As drug discovery accelerates, especially for poorly soluble small‑molecule compounds, formulation teams increasingly modify particle size, morphology and structure to...
Pouching solutions for sterile and moisture-sensitive devices

Pouching solutions for sterile and moisture-sensitive devices

Sterile pouch loading and sealing is far more complex than a conventional packaging operation: When the pouch itself becomes the primary sterile barrier (and the product...
How a manufacturer tripled granulation line productivity

How a manufacturer tripled granulation line productivity

A global manufacturer exporting to US markets was facing a 20% rejection rate for Sucralfate Tablets, leading to order non-fulfilment penalties
Measurement uncertainty explained – Why it matters more than you think

Measurement uncertainty explained – Why it matters more than you think

In regulated environments, where decisions often depend on whether a result passes or fails a defined limit, understanding measurement uncertainty becomes critical
NSF Pharma Biotech Conference Q&A highlights priorities for contamination control, quality culture and workforce development

NSF Pharma Biotech Conference Q&A highlights priorities for contamination control, quality culture and workforce development

The discussion underscored the growing importance of aligning employee behaviours with compliance objectives, while also addressing the industry’s ongoing challenges...
What is ISO/IEC 17025 and why it matters for calibration

What is ISO/IEC 17025 and why it matters for calibration

As regulatory expectations continue to increase, particularly around data integrity and traceability, the question becomes less about collecting data, and more about...

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