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Our mission

To create an environment where the global biopharmaceutical industry can collaborate in order to accelerate their rate of progress, for the benefit of all. We do this by:

Bringing leaders together
to create future visions that focus the industry’s energy on the key emerging opportunities
Mobilizing communities
of the top experts around these opportunities, up and down the biopharma value chain
Creating partnerships
that enable change and provide the quickest route to implementation and results
Replacing isolation

with collaboration so that the industry shares, learns and
builds the best solutions together

What is BioPhorum?

Unique global collaboration
Powerful vehicle for change
Industry leaders and experts working in concert
Delivers results by pooling knowledge, practices and ideas

Phorums

Industry changing initiatives

Member companies

Active participants

Thriving communities

Voice of the industry

Why BioPhorum?

We make the journey better, faster, cheaper …and results come in many ways

Quality
  • more effective compliance
  • better process control
  • lower business and supply chain continuity risk
Cost
  • lower waste
  • improved productivity
  • better investment decisions and costs avoided
Speed
  • faster approvals
  • faster batch release
  • accelerated improvement and technology adoption
Agile
  • faster capacity expansion
  • faster response
  • flexible operations supporting the product pipeline

Recent releases

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Jan 09 2022

Addressing the challenges of using RNA as a therapeutic or a gene-editing tool

RNA technologies, including mRNA therapeutics, have emerged as a promising drug modality due to their essential biological role in protein expression and their...
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Jan 09 2022

Supporting particle investigations with risk-based decision-making

BioPhorum’s Visual Inspection workstream has invested considerable time and effort to add clarity to the uncertainty around how to assess the risk of atypical particles...
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Jan 09 2022

Using a closure analysis method to reduce CGT contamination risks

Many cell therapy manufacturing processes use open unit manipulations. As a result, they are at risk of potential contamination that can result in manufacturing batch...
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Jan 09 2022

Bridging the worlds of IT and CGT through analogies

Cell and gene therapies (CGTs) have enormous potential to create personalized therapeutics for patients with diseases that were once untreatable – but they come with...
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Nov 30 2021

How to replenish working cell banks with a risk-based scientific approach

Cell banks represent the fundamental starting substrates for biological drug substance/drug substance intermediate manufacturing. So, the availability of...
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Nov 30 2021

How to make in-use stability and compatibility studies a success

In-use stability and compatibility studies are often used in biotherapeutic development to assess biologic drugs with diluents and/or administration components. The...
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