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BioPharm
January 2018
Volume 31, No. 1
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| 2018 BIOPHARMA FOCUS |

Science and Funding Inject Excitement into Biopharma

Rita C. Peters

Scientific advances and renewed investment may infuse biopharma for growth.
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FDA Drug Approvals Hit Record Levels in 2017

Cynthia A. Challener

Gene therapies highlight FDA new drug approvals in 2017.
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BioPharm International January Issue
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Drug Pricing and Quality are Top Issues for 2018

Jill Wechsler

Policy makers look to boost generic drugs, curb opioid abuse, and maintain incentives for innovation.
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What to Watch for in 2018

Jim Miller

The industry will see an impact from financing, M&As, advanced therapies, generic drugs, and the retail market in 2018.
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| UPSTREAM PROCESSING |

Expansions in Cell Culture Facility Offerings

Feliza Mirasol

Recent investments show expansion activity in cell culture facilities.
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| DOWNSTREAM PROCESSING |

Evolving UF/DF Capabilities

Cynthia A. Challener

Advances in TFF and single-use systems help advance UF/DF on the continuous processing path.
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| FLUID HANDLING |

Selecting and Installing Peristaltic Pump Tubing

Gregg Johnson

Proper selection and installation optimizes fluid system performance.
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| PEER-REVIEWED |

Using Direct Transition Analysis in Chromatography

Yuanyuan Cui, Zheng Huang, Jack Prior

The authors present a robust and easy-to-implement chromatography column performance assessment method, called direct transition analysis (DTA).
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| ANALYTICS |

Stability Testing Ensures Proper Packaging for Drug Storage

Feliza Mirasol

Conducting stability testing on APIs/finished drug product helps ensure shelf-life storage.
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| OPERATIONS |

Process Monitoring and Control Technologies Optimize Operations

Amber Lowry

New technological advancements seek to improve pharmaceutical process monitoring and control.
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| SERIALIZATION |

Bio/Pharma Serialization Nears a Tipping Point

Agnes Shanley

Open standards based on GAMP and GS1 will soon be released and more companies are moving beyond basic compliance.
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| FROM THE EDITOR |

Milestones Mark Progress and Challenges

Rita C. Peters

BioPharm International will mark 30 years of biopharma industry progress and challenges in 2018.
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| ASK THE EXPERT |

Meeting Data Integrity Requirements

Siegfried Schmitt

Enterprise-wide processes, procedures, and systems are the keys to data integrity and peace of mind, according to Siegfried Schmitt, PhD, principal consultant at PAREXEL.
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| EVENTS |

Pharmapack Europe

Feb. 7–8, 2018

IFPAC-2018

Feb. 11–14, 2018

9th Global Drug Delivery & Formulation Summit

Mar. 12–14, 2018

more events

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