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    Drug Manufacturing

    Drug Manufacturing: the process of industrial-scale synthesis of pharmaceutical drugs by pharmaceutical companies. The process of drug manufacturing can be broken down into a series of unit operations, such as milling, granulation, coating, tablet pressing, and others. FDA ensures the quality of drug products by carefully monitoring drug manufacturers' compliance with its Current Good Manufacturing Practice (CGMP) regulations.

    Webinars

    • NOV 17, 2016 | 1:00 PM
      Initiatives to advance stem cell science and medicine at California's $3 billion stem cell agency
      Initiatives to advance stem cell science and medicine at California's...
      The mission of the California Institute for Regenerative Medicine (CIRM) is to accelerate stem cell treatments to patients with unmet medical needs.  With $3 billion in funding and 300 a...
      Speaker: Stephen Lin, PhD
      Presented at: 4th Annual 24 Hours of Stem Cellsâ„¢ virtual event
      4
      NOV 17, 2016 | 9:00 AM
      From bench to BLA - a review of common regulatory questions
      From bench to BLA - a review of common regulatory questions
      This panel will discuss quality requirements of ancillary materials used in cell therapy manufacturing, relevant standards and how requirements vary by phase.  Participants will learn wh...
      Speaker: Joyce Frey-Vasconcells, PhD , Michael Mendicino, PhD , Kelli Tanzella, PhD
      Presented at: 4th Annual 24 Hours of Stem Cellsâ„¢ virtual event
      3
      NOV 17, 2016 | 5:00 AM
      Partnering to advance regenerative medicine and cellular therapies
      Partnering to advance regenerative medicine and cellular therapies
      The Alliance for Regenerative Medicine (ARM) is the preeminent global advocate for regenerative and advanced therapies. ARM fosters research, development, investment and commercialization of ...
      Speaker: Michael Werner , Morrie Ruffin, PhD
      Presented at: 4th Annual 24 Hours of Stem Cellsâ„¢ virtual event
      4
      NOV 03, 2016 | 9:00 AM
      Risk Mitigation and Management to ensure Virus Safety of Biopharmaceuticals: Regulatory Perspectives and Industry Best Practices
      Risk Mitigation and Management to ensure Virus Safety of Biopharmaceuticals:...
      DATE: November 3, 2016 TIME:  9:00AM PT, 12:00PM ET Patient safety is at the core of biopharmaceutical manufacturing operations. Ensuring virus safety of biopharmaceutical products p...
      Speaker: Hazel Aranha, PhD, RAC
      Sponsored By: Sartorius, Sartorius
      6
      MAY 04, 2016 | 5:00 AM
      Complete workflow solution from gene-to-protein
      Complete workflow solution from gene-to-protein
      Reliability from gene sequence to the expressed and purified protein is essential for many aspects of basic research and drug development. Thermo Fisher Scientific’s complete portfolio ...
      Speaker: Michael Spring
      Presented at: 2016 Gibco ExpressionWorld
      2
      APR 14, 2016 | 7:00 AM
      WEBINAR: Avoiding the Pitfalls When Automating Cell Viability Counting for Biopharmaceutical Quality Control
      WEBINAR: Avoiding the Pitfalls When Automating Cell Viability...
      April 14, 2016, 7:00am PT, 10:00am ET, 2:00pm GMT Whether cells are being used to manufacture a therapeutic drug product or for pharmacology, measuring the cell viability and concentration...
      Speaker: Tony Harrison
      Presented at: Beckman Coulter Life Sciences Virtual Trade Show
      Sponsored By: Beckman Coulter Life Sciences, Beckman Coulter Life Sciences
      10 1
      SEP 22, 2015 | 8:00 AM
      WEBINAR: SPR for Aptamer-Based Molecular Interactions in Programmable Materials
      WEBINAR: SPR for Aptamer-Based Molecular Interactions in Programmable...
      Surface plasmon resonance (SPR) is a sensitive, label-free technique that detects mass changes due to biomolecular interactions on a surface. This versatile method has been used to evaluate t...
      Speaker: Erin Gaddes, MS
      Sponsored By: Ametek, Ametek
      5
      SEP 03, 2015 | 1:30 PM
      Challenges of Natural Preservative Application
      Challenges of Natural Preservative Application
      Natural preservation is often cited as effective and “safe” alternative to traditional synthetic preservative systems. However, the so-called natural preservatives bring a number...
      Speaker: Philip Geis, PhD
      Presented at: Microbiology Virtual Event Series 2015
      2 1
      SEP 02, 2015 | 6:00 AM
      Simple, fast and accurate microbial identification by sequencing
      Simple, fast and accurate microbial identification by sequencing
      Managing microbial contaminants is critical during the manufacturing of biologics, food and beverage to ensure that products meet the high quality product standard as well as staying complian...
      Speaker: Jane Luo, PhD
      Presented at: Microbiology Virtual Event Series 2015
      9
    NOV 17, 2016 | 1:00 PM
    Initiatives to advance stem cell science and medicine at California's $3 billion stem cell agency
    Initiatives to advance stem cell science and medicine at California's...
    The mission of the California Institute for Regenerative Medicine (CIRM) is to accelerate stem cell treatments to patients with unmet medical needs.  With $3 billion in funding and 300 a...
    Speaker: Stephen Lin, PhD
    Presented at: 4th Annual 24 Hours of Stem Cellsâ„¢ virtual event
    4
    NOV 17, 2016 | 9:00 AM
    From bench to BLA - a review of common regulatory questions
    From bench to BLA - a review of common regulatory questions
    This panel will discuss quality requirements of ancillary materials used in cell therapy manufacturing, relevant standards and how requirements vary by phase.  Participants will learn wh...
    Speaker: Joyce Frey-Vasconcells, PhD , Michael Mendicino, PhD , Kelli Tanzella, PhD
    Presented at: 4th Annual 24 Hours of Stem Cellsâ„¢ virtual event
    3
    NOV 17, 2016 | 5:00 AM
    Partnering to advance regenerative medicine and cellular therapies
    Partnering to advance regenerative medicine and cellular therapies
    The Alliance for Regenerative Medicine (ARM) is the preeminent global advocate for regenerative and advanced therapies. ARM fosters research, development, investment and commercialization of ...
    Speaker: Michael Werner , Morrie Ruffin, PhD
    Presented at: 4th Annual 24 Hours of Stem Cellsâ„¢ virtual event
    4
    NOV 03, 2016 | 9:00 AM
    Risk Mitigation and Management to ensure Virus Safety of Biopharmaceuticals: Regulatory Perspectives and Industry Best Practices
    Risk Mitigation and Management to ensure Virus Safety of Biopharmaceuticals:...
    DATE: November 3, 2016 TIME:  9:00AM PT, 12:00PM ET Patient safety is at the core of biopharmaceutical manufacturing operations. Ensuring virus safety of biopharmaceutical products p...
    Speaker: Hazel Aranha, PhD, RAC
    Sponsored By: Sartorius, Sartorius
    6
    MAY 04, 2016 | 5:00 AM
    Complete workflow solution from gene-to-protein
    Complete workflow solution from gene-to-protein
    Reliability from gene sequence to the expressed and purified protein is essential for many aspects of basic research and drug development. Thermo Fisher Scientific’s complete portfolio ...
    Speaker: Michael Spring
    Presented at: 2016 Gibco ExpressionWorld
    2
     
     
  • APR 14, 2016 | 7:00 AM
    WEBINAR: Avoiding the Pitfalls When Automating Cell Viability Counting for Biopharmaceutical Quality Control
    WEBINAR: Avoiding the Pitfalls When Automating Cell Viability...
    April 14, 2016, 7:00am PT, 10:00am ET, 2:00pm GMT Whether cells are being used to manufacture a therapeutic drug product or for pharmacology, measuring the cell viability and concentration...
    Speaker: Tony Harrison
    Presented at: Beckman Coulter Life Sciences Virtual Trade Show
    Sponsored By: Beckman Coulter Life Sciences, Beckman Coulter Life Sciences
    10 1
    SEP 22, 2015 | 8:00 AM
    WEBINAR: SPR for Aptamer-Based Molecular Interactions in Programmable Materials
    WEBINAR: SPR for Aptamer-Based Molecular Interactions in Programmable...
    Surface plasmon resonance (SPR) is a sensitive, label-free technique that detects mass changes due to biomolecular interactions on a surface. This versatile method has been used to evaluate t...
    Speaker: Erin Gaddes, MS
    Sponsored By: Ametek, Ametek
    5
    SEP 03, 2015 | 1:30 PM
    Challenges of Natural Preservative Application
    Challenges of Natural Preservative Application
    Natural preservation is often cited as effective and “safe” alternative to traditional synthetic preservative systems. However, the so-called natural preservatives bring a number...
    Speaker: Philip Geis, PhD
    Presented at: Microbiology Virtual Event Series 2015
    2 1
    SEP 02, 2015 | 6:00 AM
    Simple, fast and accurate microbial identification by sequencing
    Simple, fast and accurate microbial identification by sequencing
    Managing microbial contaminants is critical during the manufacturing of biologics, food and beverage to ensure that products meet the high quality product standard as well as staying complian...
    Speaker: Jane Luo, PhD
    Presented at: Microbiology Virtual Event Series 2015
    9
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