PharmaCyte Biotech in final audit of manufacturing site
PharmaCyte Biotech said Monday that cGMP Validation, the company’s GMP consultant, is conducting its final audit of the manufacturing facility…
Pharmaceuticals, Biotechnology and Life Sciences
PharmaCyte Biotech said Monday that cGMP Validation, the company’s GMP consultant, is conducting its final audit of the manufacturing facility…
Puma Biotechnology, Inc. (NASDAQ: PBYI), a biopharmaceutical company, announced that its licensing partner CANbridge Pharmaceuticals, Inc. has received marketing approval of NERLYNX® (neratinib) in mainland China from the National Medical Products Administration (NMPA) of China.
DongWha Pharm’s said it is getting ready for second phase of clinical trials of new drug candidate DW2008 to treat COVID-19.
CHEONGJU, South Korea–(BUSINESS WIRE)–#BIOKOREA—BIO KOREA 2020 International Convention, where global bio experts correspond, is shifting to an online-only event.
Satralizumab monotherapy significantly reduced risk of relapse in patients with NMOSD, following a previous positive study where satralizumab was added to baseline immunosuppressant therapy.
Yokogawa has developed the SU10 Single CellomeTM Unit, a device that uses a nanopipette*1 to inject substances such as genes and drugs and aspirate intracellular materials at target locations in individual cells
– Results published in first paper from 18-month analysis of ongoing pivotal Phase 3 trial were generally consistent with overall…
BioNTech SE said Monday its development a potential vaccine to induce immunity and prevent COVID-19 infection in response to the growing global health threat posed by the disease has seen rapid progress. BioNTech’s product candidate, BNT162, is a potential first-in-class mRNA vaccine in the worldwide effort against COVID-19.
The World Health Organisation has issued a guideline to keep safety in schools. We have outlined the most important keys…
Hutchison China MediTech Limited said on Friday that it got approval from the China’s authority, the Center for Drug Evaluation (CDE) of China’s National Medical Products Administration (NMPA), a Priority Review status to the New Drug Application (NDA) for surufatinib, for the treatment of patients with advanced non-pancreatic neuroendocrine tumors (NET).