White Papers
Foresight in Focus: Accelerating OSD Development with a Global Predictive Approach
In the rapidly evolving world of oral solid dose (OSD) development, foresight is not just an advantage – it is a necessity.
Precision in Every Detail: Enabling Seamless Tech Transfers through Strategic Packaging and Expert Execution
Discover how the smallest formulation details can shape the biggest outcomes in our exclusive whitepaper on accelerating pharmaceutical product launches through optimized tech transfer and packaging strategies.
Unlock Smarter Lifecycle Strategies for Injectable Therapeutics
As the injectable drug market continues to expand - driven by the rise of biologics, biosimilars, and patient-centric therapies-pharmaceutical companies face increasing pressure to differentiate their products, reduce costs, and optimize delivery systems.
Boosting biomanufacturing with optimized cell culture media: Comparing animal-derived cholesterol with synthetic PhytoChol® BioPharma
In modern biomanufacturing, consistency, purity, and safety are critical—especially when producing therapeutic proteins, vaccines, and viral vectors.
Precision That Meets Regulation—Mastering Weighing Standards in Pharma
Accurate weighing is fundamental to pharmaceutical quality and compliance. This white paper offers a detailed look into the requirements outlined in USP Chapters <41> and <1251> and European Pharmacopoeia Chapter 2.1.7, which govern how balances should be calibrated, tested, and operated in pharmaceutical labs. These standards are essential to ensuring that sample weights are accurate, repeatable, and traceable—critical to drug formulation, quality control, and regulatory audits.
sartorius-cubis-pharma-compliant-by-design
The Cubis® II lab balances meets the rigorous compliance needs of modern pharmaceutical environments. With advanced modularity, seamless data handling, and full support for 21 CFR Part 11 and EU Annex 11, Cubis® II empowers labs to achieve data integrity, audit readiness, and operational efficiency—all by design.
Trust Begins with Traceability—Why Accredited Calibration Matters
When precision and compliance are non-negotiable, choosing accredited calibration services becomes essential. This white paper from Sartorius explores the value of ISO/IEC 17025-accredited calibration laboratories and how their certificates provide validated traceability to national and international standards.
Get Reliable Weighing Results with Confidence—Master Minimum Sample Weight Requirements
When dealing with micro-quantities and strict regulatory demands, even small deviations in weighing can lead to significant errors. This expert white paper from Sartorius dives deep into the concept of minimum sample weight, a critical factor for ensuring weighing accuracy, process reliability, and compliance in pharmaceutical and laboratory environments.
New Modalities, New Tools: Choosing a Flexible Digital Platform for Drug Discovery
As pharmaceutical innovation rapidly evolves, the complexity of data generated from RNA therapeutics, gene therapies, antibody-drug conjugates (ADCs), and protein degraders necessitates a new approach to digital infrastructure.
Design Smarter Dose Strategies for Adaptive Clinical Trials
In an era of precision medicine and adaptive clinical trial designs, dose flexibility is no longer optional—it’s essential. From preclinical development to commercialization, the ability to scale, modify, and tailor dose strengths is key to meeting regulatory expectations and optimizing patient-centered therapies.
