Teva North America
1090 Horsham Road
North Wales, PA 19454 USA
As part of the Actavis Group we have been able to develop one of the broadest product portfolios and strongest pipelines in order to provide a constant flow of the latest generics for our customers.
Our organisation is built on a strong heritage of local manufacturing with more than 5 billion tablets being produced per year at our manufacturing facility in Devon, a program of significant investment has ensured we are well equipped to support the supply chain demands of our customers both now and in the future .
Actavis UK strive to bring value and innovation to our customers through our Partner Pricing scheme, the professional support available through our Actavis Academy combined with a focus on great customer service.
Actavis Biologics Ltd is the Global Centre of Excellence for the development and manufacture of all biologic medicines. Delivering process and product development; cGMP manufacturing of biologics and quality/regulatory expertise from a custom-designed facility located in Liverpool, UK. With well over a decade of experience in producing a wide range of complex biopharmaceuticals, the biologics team provides Actavis with a strong foundation for establishing a leadership position in global biologics.
Biosimilars represent one of the pillars of Actavis’ strategy to drive long-term growth and the Company is committed to building a leadership position in the emerging global biosimilars market. We believe that biosimilars are the next frontier in the evolution of healthcare.
In Liverpool, we are currently working on a number of biologics programmes.
More information on Actavis’ Biosimilars R&D
Actavis is focused on product safety and conducts comprehensive safety monitoring and evaluations throughout all stages of our product lifecycle.
With patient safety a primary concern, we encourage healthcare professionals and patients to report any adverse event which may occur in relation to an Actavis product. An adverse event includes reports of any side effect, product misuse, abuse or overdose, including inappropriate use by children or women who are pregnant or breast-feeding. It also includes reports of a product that was used for something other than the intended purpose or was ineffective, given with another medicine or any complaints relating to the product.
Adverse events should be reported either directly to The Medicines and Healthcare Products Regulatory Agency (MHRA) through its Yellow Card reporting system or you can contact Actavis Medical Information directly on 01271 385257.
If you have any medical queries or any feedback you would like to give us, please use the Medical Information Feedback form below, and we will be pleased to get back to you.
Combined Oral Contraceptives:
We have elected to work with three “Community Partners”, which allows us to build relationships and really make a difference. Our Community Partners are all registered charities and are in line with our business strategy of improving health and quality of life
Actavis is proud of its commitment to enhancing the quality of life in our communities. As part of this focus, we dedicate meaningful resources to several Social and Environmental Responsibility programs around the world.
A focused Corporate Giving program provides financial support to global not-for-profit organisations aligned with our mission and core businesses. And a global Environmental Responsibility program ensures that our Company is doing its part to lessen the impact of our business on the environment.
Actavis Responsibility harnesses the power of our engaged and passionate global employees and the resources of our global Company to drive the understanding and reality that “Together We Make a Difference.”
The Actavis Schemes provide over 950 medicines to registered healthcare professionals across hospitals, pharmacies and dispensing doctors. If you are a healthcare professional you will find details of our various schemes to the left of this page.
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