Writing

Notes from downstream.

Short technical articles on purification, validation and where biomanufacturing is heading. Written from the floor, not the brochure.

Digital Biomanufacturing & AI

The Potential of Artificial Intelligence in mAb Downstream Processing

How Artificial Intelligence and Machine Learning are transforming downstream purification of monoclonal antibodies (mAbs). Mechanistic hybrid modeling, digital twins, and predictive PAT by Mehrdad Khani.

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Process Intensification

Continuous Chromatography & PAT in Modern Biomanufacturing

Explore multi-column continuous chromatography (MCC) and real-time PAT in modern biomanufacturing. Downstream process intensification insights from Mehrdad Khani.

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Downstream Purification

Overcoming Host Cell Protein (HCP) Clearance Bottlenecks in Biosimilar Processing

Advanced strategies for Host Cell Protein (HCP) clearance and residual impurity reduction in biosimilar downstream manufacturing. Insights by Mehrdad Khani.

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GMP & Validation

Cleaning Validation in Multi-Product Biomanufacturing: Calculating MACO & CIP Verification

Mastering Cleaning Validation in multi-product biomanufacturing suites. Maximum Allowable Carryover (MACO), TOC recovery studies, and CIP verification by Mehrdad Khani.

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Complex Biologics

The Rise of Bispecific Antibodies

Overcome downstream purification challenges for bispecific antibodies. Advanced chromatography and filtration techniques by Mehrdad Khani.

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Biomanufacturing Trends

The Future of Monoclonal Antibodies

Explore the future of Monoclonal Antibodies (mAbs) and their impact on Canada's biomanufacturing sector. Insights from Mehrdad Khani, Bioprocess Engineer.

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Quality by Design

Implementing Quality by Design (QbD) in Biomanufacturing

A comprehensive guide to implementing Quality by Design (QbD) in biopharmaceutical manufacturing. Ensure consistent quality for Health Canada approvals.

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Viral Safety & Filtration

Viral Clearance Strategies in Downstream Processing

Robust viral clearance and inactivation strategies for biopharmaceuticals. Meet regulatory requirements for Health Canada and FDA with effective downstream processing.

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Filtration & Scale-Up

Scaling Up Tangential Flow Filtration

Learn best practices for scaling up Tangential Flow Filtration (TFF) in biomanufacturing. Essential downstream strategies for CDMOs in Canada and North America.

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Chromatography & Affinity

Troubleshooting Protein A Chromatography

Discover key troubleshooting techniques for Protein A Chromatography in downstream bioprocessing to ensure high yield and GMP compliance in Canada.

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Downstream Processing

Optimizing Ion Exchange (IEX) Chromatography

Maximize API production yields by optimizing Ion Exchange (IEX) chromatography. Advanced purification strategies for GMP biomanufacturing.

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