PHARMA ONLINE WHITE PAPERS

• Selecting The Best Deterministic Method For Your CCIT Project

  Container Closure Integrity Testing (CCIT) ensures drug sterility, evolving with regulatory updates like USP <1207>. Deterministic methods are preferred over probabilistic ones to maintain product integrity.

• Is Sustainability The Key To Agile Biopharma Manufacturing?

  3/18/2025

  In biologics manufacturing, change is constant. Discover how new innovations and a focus on sustainability have gotten 62% of executives to prioritize eco-friendly practices, which reflects a commitment to long-term viability.

• Meet Regulation Requirements With RTU Vials And Cartridges

  10/9/2025

  Sterile manufacturing remains vital, with resilient supply chains preventing shortages. Industry and regulators prioritize integrity as demand surges, making it the fastest-growing pharmaceutical segment.

• Finding An Optimal Harvest Solution By Considering Both Cost And Sustainability

  3/27/2025

  Optimize your bioprocessing harvest with single-use centrifugation. Reduce costs, waste, and space needs compared to traditional depth filtration methods.

• Streamline Your mAb Manufacturing With Strategic Development And CDMO Compatibility

  6/4/2025

  Though the journey to mAb development begins at lab scale, for clinical trials and commercial distribution, a production process must be streamlined and scalable to 2,000 L production and above.

• The Future Of DMTA In Drug Discovery And Development

  5/28/2026

  AI‑enabled DMTA cycles connect design, experimentation, and analysis through structured data and automation, reducing manual handoffs while accelerating discovery, development, and CMC decision‑making.