PAN-Biotech · PAN-Celltech

The Open Downstream

A qualified GMP product for every step - standard, scalable, customizable. One roof, from bench to patient.

Why downstream

Where the cost and the risk concentrate

Downstream processing carries well over half of a biologic's production cost, and it is where a single mistake is most expensive to unwind. The buffers, stock solutions and water that run through it deserve a qualified partner, not a commodity buy - one that covers every step, scales with the programme and stays consistent from bench to patient.

The process

A qualified product for every downstream step

Seven steps, from harvest to release - the universal stock solutions recur across them, so the same qualified article serves many steps.

  1. 1Harvest & clarificationDPBS 1x / 10x, WFI water
  2. 2Capture - Protein ANaCl 5 M, Tris 1 M, Citrate, Glycine
  3. 3Viral inactivation (low-pH)Citrate 100 mM pH 3.0, Tris 1 M
  4. 4Polishing - IEX / HIC / SECAcetate, Phosphate, Amm. sulfate, Histidine, NaOH
  5. 5Ultrafiltration / diafiltrationHistidine, Sucrose, Trehalose, PS20 / PS80
  6. 6FormulationHistidine, Sucrose / Trehalose, PS20 / PS80, NaCl 5 M
  7. 7QC & releaseCertificate of Analysis, DMF support, stability
The portfolio

The standard portfolio, by function

One stocked size per product (500 ml or 100 ml) with its article number; 1000 ml bottles and 1-1000 L single-use bags on request; a WFI Beyond version of every buffer on request. 32 products across six functional families, each linked to its own product page (click any row). The same products are grouped under Products › Downstream / DSP.

Foundation - water & isotonic bases3 products
Salts & ionic-strength stocks4 products
pH / buffering stocks8 products
Chelation, lysis & nucleic-acid clearance6 products
CIP, sanitisation & storage2 products
Stabilisers & formulation excipients9 products
One roof

One partner, four options, four applications

WFI Beyond - the premium quality ceilingopt-in across the range
One roof, one partnerRUO to GMP · from bench to patient
EU Annex 1 GMP · ISO 9001 · filed FDA DMFs · audit-ready · dispatched in 24 h
Every stepA qualified GMP product for every downstream step - test it and build your own formulations.
Scale500 / 100 ml stocked; 1000 ml bottles and bags to 1000 L on request. Matched RUO to GMP - qualify once.
CustomA fully customized GMP formulation at any step - without switching supplier.
Quality & documentationA Certificate of Analysis on every lot; DMF support on DPBS and WFI Beyond; audit-ready.
Proven with customers

Case studies

Real, anonymised proof from PAN's GMP downstream and supply partnerships.

Case study · OEM

A two-year OEM bridge, delivered under pressure

A regulatory shutdown took a global supplier's US site offline. PAN bridged ~25 products - ~300,000 bottles over ~2 years, no rejections recorded.

Read the case study
Case study · Vaccine

~50,000 L of GMP supply in under five weeks

Quote in 3 days; ~50,000 L delivered in under five weeks from first production, to GMP.

Read the case study
Case study · mAb

From in-house buffer prep to a qualified GMP supply partner

A monoclonal-antibody developer moves from making its own buffers to one audited GMP source.

Read the case study
Case study · Supply

Securing supply after a supplier discontinuation

An incumbent supplier exited; PAN took the RUO product end-to-end under PAN Complete.

Read the case study
Case study · CMO / CDMO

A private-label GMP line for Europe

A global brand launched a private-label GMP (EU Annex 1) line - without building a plant.

Read the case study

See all case studies in the Knowledge Hub

The thinking behind it

Whitepapers

Commercial

The Open Downstream

Why downstream is where cost, quality and regulatory risk concentrate - and how owning the options takes the risk off the table.

Read the paper
Technical

Beyond Compendial - Buffers & Reagents

The impurity dossier - elemental impurities, residual solvents, nitrosamines, leachables - mapped to mAb, mRNA, cell & gene and vaccine.

Read the paper
Practical · Make or buy

From Bench to GMP

The make-versus-buy decision for process buffers - the five hidden costs of staying in-house at GMP scale, and how to organise the switch.

Read the paper
Foundation · Water

WFI Beyond

Water for Injection engineered beyond the compendial monograph - the opt-in quality ceiling under every buffer.

Read the paper
Questions

Frequently asked questions

What is the Open Downstream range?

It is PAN-Biotech's complete GMP downstream (DSP) system: a qualified stock solution, buffer or reagent for every step of a biologic purification - capture, viral inactivation, chromatographic polishing, ultrafiltration / diafiltration and final formulation - manufactured by PAN-Celltech. One partner, from bench to patient.

Do you have a GMP product for every downstream step?

Yes. A small set of universal stock solutions - NaCl 5 M, Tris 1 M, citrate, acetate, phosphate, histidine and the water beneath them - recurs across step after step. Standard items are in stock; custom GMP formulations cover the process-specific tail.

Where can I see each product?

Every catalogue product below links to its own product page with composition, pack size and article number. The same products are also grouped under Products > Downstream / DSP.

Which buffer is used for Protein A elution?

Citrate Buffer 100 mM, pH 3.0 (CT-62500) is the standard low-pH elution buffer, and it doubles as the low-pH viral-inactivation hold. Glycine 100 mM, pH 3.0 (CT-69500) is the alternative.

What pack sizes are available?

Each standard product is stocked in one defined pack size with its own article number - 500 ml for high-volume buffers, salts, CIP reagents and water; 100 ml for concentrated excipients and additives. 1000 ml bottles and single-use bags from 1 L to 1000 L are available on request.

Can I get the buffers beyond compendial?

Yes. Every downstream buffer is also available in a beyond-compendial version produced with WFI Beyond - Water for Injection engineered beyond the Ph. Eur. / USP monograph - on request. WFI Beyond is opt-in, ordered exactly where a molecule needs it.

Can you make a custom formulation?

Yes. At any step a standard product can become a fully customized GMP formulation manufactured by PAN-Celltech to your own recipe - without switching supplier or restarting qualification.

Are the products GMP grade?

The core range is catalogue GMP, manufactured by PAN-Celltech to GMP in an EU Annex 1 facility within an ISO 9001 quality system, with a Certificate of Analysis on every lot. DPBS (CT-36500) and WFI Beyond are additionally backed by filed FDA Type IV Drug Master Files.

How fast do you ship?

Standard in-stock catalogue items are dispatched worldwide within 24 hours of order. Larger formats and custom or beyond-compendial versions are produced to order.

Open the downstream for your programme

Request a product, a Certificate of Analysis, a WFI Beyond specification or a custom GMP quote - for antibody, mRNA, cell & gene or vaccine processes.

Related: WFI Beyond · PAN-Biotech GmbH · PAN-Celltech GmbH (GMP arm / manufacturer of record). GMP-compliant, audit-proven; EU Annex 1 is a capability, not a certification.