| MANUFACTURING |

Forty Years of Drug Product Manufacturing Advances

Oral solid-dosage and parenteral drug manufacturing equipment and systems have made great strides in safety and efficiency.
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| ANALYTICAL TESTING |

Advances in Analytical Testing Tools for the Bio/Pharma Industry

Industry experts discuss how advances in analytical testing tools have helped address challenges in pharmaceutical analysis.
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| PEER-REVIEWED RESEARCH |

Analysis of Total and Transferrin-Bound Iron from Serum Samples

Incorporating structural constraints into pharmacokinetic studies of iron sucrose formulations.
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| DRUG DEVELOPMENT |

Data Integrity Expectations of EU GMP Inspectors

The author reviews key technological expectations of EU GMP inspectors on the integrity of e-records.
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| EU REGULATORY WATCH |

A Question of Quality

Greater transparency and reliability of information are needed in the quality assessments of biosimilars.
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| OUTSOURCING REVIEW |

Contract Manufacturing Through the Years

How has the bio/pharmaceutical contract manufacturing industry evolved over the years and what does the future hold?
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| API SYNTHESIS & MANUFACTURING |

Overcoming Excipient Challenges in Spray-Dried Dispersions

Polymers and surfactants impact stability and long-term performance.
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| PACKAGING FORUM |

Packaging Improves Medication Adherence

A staggering percentage of people do not take their medication correctly, but pharmaceutical packaging aims to improve patient compliance using new technology to address reasons for non-adherence.
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| ASK THE EXPERT |

Inspections: The Value of the Opening Presentation

The opening presentation gives the company a chance to put their best foot forward, according to Siegfried Schmitt, principal at PAREXEL.
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