Industry news

  • 06 December 2017

    What makes a modern-day biotech?

    FierceBiotech

    If biotechnology is the use of living cells and molecules to make biological products, does this mean all companies producing biological products or solutions are classified as a biotech?

  • 06 December 2017

    About 0.5 trillion rubles are allocated for procurement of VED drugs in Russia

    GMP News

    Notwithstanding the market economy, the state must constantly monitor the prices of medicines, because this issue concerns everyone who lives in Russia. This statement was made by Prime Minister Dmitry Medvedev in his interview with Russian TV channels.

  • 05 December 2017

    Russian government will support drug compounding

    GMP News

    Russian government will give its backing to a drug compounding. Senators and experts discussed this matter in the press centre of “Parliamentary Gazette” – the official gazette established by Russia’s Federation Council.

  • 05 December 2017

    WHO published its study report on falsified medical products

    GMP News

    An estimated 1 in 10 medical products circulating in low- and middle-income countries is either substandard or falsified, according to new research from World Health Organization (WHO).

  • 04 December 2017

    Ferring and Ache Laboratorios Farmaceuticos open a joint nanotechnology centre

    GMP News

    Ferring Pharmaceuticals and Aché Laboratórios Farmacêuticos, a Brasilian pharmaceutical company, announced the inauguration of their joint nanotechnology centre in São Paulo, Brazil. Focused exclusively on nanotechnology research and development, the centre forms the first phase in a long term collaboration to optimise patient care through enhanced drug delivery systems and product solutions.

  • 04 December 2017

    Russian market of non-opioid analgesics and antipyretics reaches 22.3 billion rubles

    GMP News

    Since 2015, the sales of non-opioid analgesics and antipyretics have fallen significantly in physical terms, but are still growing, if calculated based on prices of final consumption, according to retail audit data released by IQVIA.

  • 01 December 2017

    Draft law on accelerated registration of foreign medicines approved in Russia

    GMP News

    At a meeting held on November 23, 2017, the Government of the Russian Federation approved the draft federal law “On Amendments to the Federal Law on the Circulation of Medicines” and decided to submit it to the State Duma in accordance with the established procedure.

  • 01 December 2017

    How much is an FDA shortcut worth to drug developers hustling to an OK? Holding steady at $125M, cash

    John Carroll / Endpoints News

    The market for priority review vouchers is holding steady at $125 million per deal. That’s what BioMarin just received for its PRV, sold off to an unidentified buyer looking to slash 4 months off of a regular drug review. And it’s close to twice what the company reaped in 2014 when they sold their first PRV to Regeneron $REGN for $67.5 million.
  • 29 November 2017

    Authorities decide to simplify the entry of foreign drugs to the Russian market

    GMP News

    According to the Russian Ministry of Industry and Trade, this institution has prepared the draft law “On Amendments to the Federal Law On Circulation of Medicines”, intending to reduce time required for foreign medicines to enter the Russian market.

  • 29 November 2017

    EMA published a set of GMP guidelines for advanced therapies

    GMP News

    The European Commission has published a set of guidelines on good manufacturing practice (GMP) specific to advanced therapy medicinal products (ATMPs). ATMPs are medicines for human use that are based on genes or cells. These therapies offer ground-breaking new opportunities for the treatment of diseases and injuries. They are particularly important for severe, untreatable or chronic diseases for which conventional approaches have proven to be inadequate.

All Portfolio

MEDIA CENTER