The French National Agency for Medicines and Health Products Safety (Agence nationale de sécurité
du médicament et des produits de santé – ANSM), was created by the Act of 29 December 2011 relating to the increased safety of medicines and healthcare products.
Accelerate Cell-Line Development
The optimal development of cell lines to provide protein-based medicines for applications targeting diseases in humans is essential for increased efficiency and lowering final cost of goods.
Biotechnology Industry Organization (BIO) is the world's largest biotechnology organisation.
A newsletter for biotech managers covering corporate strategy and management questions.
BioCentury TV: Biosimilar Report Card - Learnings from Europe
While the U.S. is still waiting for low-cost versions of biologic drugs, a biosimilars marketplace has been operating in Europe for past the seven years. Is it working as planned?
BioSpace is the leading online community for industry news and careers for life science professionals.
A monthly, controlled-circulation magazine devoted to the development, scale-up, and manufacture of biotherapeutics and biodiagnostics
The latest on biotech & pharma deals, clinical trials, FDA decisions, and key regulatory issues.
The Korean Food and Drug Administration (KFDA) resembles the FDA of the United States. It was established in 1998 and regulates foods, pharmaceuticals, medical devices and cosmetics.
Kemi Världen Biotech
The website for the Kemivärlden Biotech Chemical Journal, news for all who work with chemistry or biotechnology in industry or academia.
Life Science Sweden
Life Science Sweden is Scandinavia's largest newspaper on biotechnology, monitoring new scientific knowledge, technology, finance, stock market, ethics, patents and bioinformatics.
Manufacturing Chemist reports on current and future trends in the global marketplace, including the latest developments in drug discovery, biotechnology, drug delivery, ingredients, processing technologies and equipment, packaging, business strategies and regulatory updates.
The main regulatory body for creating laws and standards for medical devices and drugs in Japan is the Ministry of Health, Labour and Welfare (MHLW). Under the MHLW is the Pharmaceutical and Food Safety Bureau. This bureau is in charge of setting pharmaceutical and medical device regulatory policy.
The Medicines and Healthcare products Regulatory Agency (MHRA) is the government agency which is responsible for ensuring that medicines and medical devices work, and are acceptably safe. The MHRA is an executive agency of the Department of Health.
The Medical Products Agency (MPA) is the Swedish national authority responsible for regulation and surveillance of the development, manufacturing and marketing of drugs and other medicinal products.
Pharmaceutical Business Review
The Pharmaceutical Business Review website is your number one stop for all the latest news, comment and industry information, offering content that is produced by a dedicated team of journalists and global industry experts.
Pharmaceuticals and Biopharmaceuticals Innovation Hub
The Pharmaceutical and Biopharmaceutical innovation hub brings together expertise in a range of physical and biological sciences to pioneer innovative approaches to drug discovery.
Pharma IQ, a division of IQPC, is an international online community focusing on providing pharmaceutical professionals with knowledge, information and articles. We are dedicated to creating a learning environment for sharing ideas, best practices and solutions within the pharmaceutical community.
TAP Biosystems is a leading global provider of automated cell culture and fermentation systems to the bio-pharma, regenerative medicine and industrial biotechnology sectors.