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Touchlight becomes the first synthetic DNA API manufacturer to receive GMP certification
The CDMO's Hampton, UK facility has received GMP certification to produce investigational APIs and critical starting materials for DNA vaccines and non-viral gene therapies
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Managing airflow, contamination risks and technician well-being with biological safety cabinets
Microbiology labs and other facilities researching biohazardous materials and pathogens such as bacteria, viruses and fungi must avoid contamination. It is critical to ensure...
Daiichi Sankyo and BioMed X Institute join forces to develop multi-specific biologics for cancer therapy
Through this collaboration, they aim to discover and develop novel target combinations for bi- and multi-specific biologics for the treatment of solid tumours
Teva Pharmaceuticals, Klinge Pharma and Formycon join forces to commercialise Eylea biosimilar
FYB203, which will be marketed under the name AHZANTIVE®3 if approved by the EMA, will be commercialised by Teva Pharmaceuticals in the majority of Europe and Israel
Vetter launches new iteration of the V-OVS syringe closure system
The new version is optimised to protect the integrity of the injectable product with easier handling characteristics and an intuitive opening mechanism
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Global ampoules and blister packaging market expected to be worth US$14.81bn by 2020, finds report
Blister packaging expected to be highest growing material for pharma products in North America
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