Market News

The exclusive launch of Teva's generic version of Reyataz marks the company's fifth generic product offering for the treatment of HIV-1 infection.

First and only CML therapy with Treatment-free Remission data in its label.

Clinical studies showed 95% symptom improvement at one minute and reduced redness for up t 8 hours.

iMatrix recombinant Laminin-511 E8 protein fragments permit ES/iPS cells to be maintained in xeno-free, feeder-free culture conditions enabling easy application in medical trials.

Allergan plans to file petitions for rehearing of the appeals court decision and has asserted a new Orange Book patent against Sandoz's generic version of Combigan.

Merger integrates Crown Bioscience’s leading translational technology platform providing drug target validation, efficacy testing and patient response characterization with JSR’s IVD solutions, GMP manufacturing capabilities and worldwide distribution ...

New collaboration agreement to identify new antisense oligonucleotide drug candidates.

First and only FDA-cleared PK dosing software to support healthcare professionals in creating personalized dosing regimens for patients 16 and older with hemophilia A.

Integration of supply chain a critical issue as industry globalises, with a resurgence in European manufacturing and biotech markets forecast.

Truxima is mAb biosimilar to Roche's MabThera (rituximab).

Total cost base to be reduced by $3 billion by the end of 2019.

Targeted formulas support symptoms before, during and after menopause.

Companies will strive to make diabetes management easier through effective use of connected devices and a diabetes management software platform.

Drug trials provide mind-blowing results.

Freeze-dried, or lyophilized, formulation aims to improve supply management by providing the same dosing regimen as liquid Oncaspar but with a three-times longer shelf life of up to 24 months.

First clinical candidate, HPN424, is in development for the treatment of metastatic prostate cancer and expected to enter Phase I clinical trials in 2018.

Service complements existing services for this testing, to provide comprehensive analysis and characterization solutions for clients involved in the production and manufacturing of biopharmaceutical products.

New version of SIMCA -advanced data analytics and visualization program - unlocks the hidden gems that hold the secret to better decision-making and greater business success.

Investment builds on company's expertise in small molecule analysis and the use of LC/MS-MS techniques.

The development will help meet growing global demand for albumin.

The design, planning and building work commences immediately and will deliver a purpose-built, dual-stream facility.

Public and private investors look set to remain supportive of innovative, early-stage drug developers.

A highly automated system to speed up testing, improve reproducibility, and enhance data output and recording.

Since the MAH pilot launch, the company has undertaken eight development programs.

Company executing long-term strategy to develop broad manufacturing capabilities for both vector supply and drug product supply to support clinical development and commercialization across pipeline.

MSD's announcement to establish UK Discovery Centre in London an 'endorsement' of the government's Industry Strategy.

Recipharm's four French facilities now serve over 50 of its customers worldwide, including a number of top 20 pharma firms.

CDMO's serialisation capabilities in place ahead of US deadline to avoid potential problems for our customers.

The Stax mAx, a single-use harvesting platform, minimizes the impact of process variability between batches.

Offers customers a comprehensive, risk-based approach to the monitoring of data quality throughout the course of a study.

Amgen launches the Enbrel Mini single-dose prefilled cartridge with AutoTouch reusable autoinjector, which is ergonomically designed for patients.

The acquisition will facilitate the growth of Shanghai Pharma's pharmaceutical manufacturing business.

Unique training courses designed around real-life situations, with hands-on access to enabling technologies.

Germany tops quality-ranking categories in the inaugural CPHI Global Pharma Index.

Quotient Sciences Translational Pharmaceutics platform integrates formulation development, real-time adaptive GMP manufacturing and clinical research.

Perception of India’s API manufacturing seems to be improving.

Experts at ADC Bio warn of impending problems in the ADC pipeline with millions wasted in development costs.

The upgraded BRS simulators make it even easier to apply specified inhalation profiles during OIP testing.

Controlled-release technologies will continue to be focal point, whereas techniques to improve solubility are likely to gain popularity.

The pharmaceutical service provider will be better positioned to support local and global customers, helping them to meet stringent development, manufacturing and packaging requirements of their injectable drugs.

Company's decision affects approximately 225 staff, specialised in tablet manufacturing, and in sachet and stick pack filling, primarily for powders and granules.

Two 500-gallon glass-lined reactors installed to reduce potential bottlenecks.

The process, which uses significantly less materials than the manual alternatives, will ultimately improve drug developers’ clinical pathway.

Financing to advance its pipeline of neoantigen cancer-based immunotherapies to the clinic.

Economic and political turmoil along with inefficient patent laws and drug pricing policies are major barriers.

Combined technology assets will provides pharmaceutical and biotech customers the unique opportunity to select a tailored expression system.

Company says it has found "no evidence of price fixing on the part of Mylan or its employees".

Acquisition would add Lutathera, a first-in-class RadioLigand Therapy approved in Europe and under review in the US for neuroendocrine tumours.

TraceLink selected for its demonstrated EU and country compliance capabilities and enterprise scalability.

Forté Pharma expands its energy and health segments with the launch of eight references in the French market, as a result of its product development strategy.

Accelerated approval of Bruton tyrosine kinase inhibitor in MCL marks AstraZeneca's entry into the treatment of blood cancers.

Company now boasts having the highest quality standards from both its in-house manufacturing and its external partners, who are also audited and certified.

£4 million investment will allow the Biopharmaceutical Product Testing business to expand its finished product and raw materials testing and increase capacity to deal with higher volumes.

Micro-Sphere adds GEA PSD-3 spray dryer in response to increased demand in spray drying.

Biogen and Ionis receive 2017 Prix Galien USA Award for extraordinary achievement in scientific innovation.

New event to create unique synergies between the parallel worlds of large, small molecules and contract services.

Court finds all claims of Teva's patent relating to Copaxone invalid based on obviousness.

Company recognised for its innovative approach to assay development, which provides customers with a portfolio of off-the-shelf assays, saving them time and money.

19 winners chosen from 200 entries, received from nearly 30 countries worldwide.

Experts state pharmaceutical regulation will shift due to increased data dependence, warn regulatory oversight is slowing six sigma adoption, and forecast increased generic options 2025 onwards.

Country accounts for over 20% of global production with $20 billion exports forecast by 2020.

The Lisbon facility brings the CDMO to over a third of the way through its implementation project.

Additional capacity enables the company to take on new customer projects, as well as offering the flexibility for projects to be transferred in from other Cambrex sites.

Investment is part of the company's anticipated $850 million in US capital projects in 2017.

Investment will contribute to a one-stop solution approach for customers.

Comprehensive 2-day event takes attendees through the most common problems found in modern tablet production, from sticking and picking to weight control and capping.

Company eligible to receive royalties from Novartis on net sales of the product.

Semaglutide receives positive 16-0 vote in favour of approval from FDA Advisory Committee.

Experts predict PAT/QbD and CM adoption may take 10 years, with smaller generic players to drop out of the market if unable to innovate in time.

TraceLink, Sharp and Major Pharma Brand to discuss trade partner connectivity at CPHI Worldwide.

New European Council will support RAPS’ growing member base and volunteer network across Europe to ensure compliance with global regulations and to drive regulatory excellence

The center will allow STA to introduce transition metal catalyst-screening technology to their existing small-molecule process development and manufacturing platform.

The partnership will be able to cater to virtually all customer needs for viral vector services, from initial vector engineering and development to GMP production.

US District Court for the Eastern District of Texas decides all asserted claims of the patents relating to Restasis invalid based on obviousness.

Combination creates diversified pharmaceutical company with 5th largest generics business in the US.

Investments will help the company to bring candidate biopharmaceuticals from bench to clinic.

Future acquisitions will not be dominated by big deals and large mergers, but rather smaller commentary services and niche technologies to fill specific technology asset gaps.

Project will build upon the results of Phase II trials undertaken by Bavarian Nordic.

Croda on hand at CPHI to increase API delivery and improve API stability.

Investments include the installation of development and analytical equipment to support the development of highly potent APIs.

Compact and high-speed powder filling