Saxsons Group

Knowledge Hub · CRP™ Dispensing System

The automation inside the cell — not the cell itself.

CRP isn\'t a shielded hot cell. It\'s the dispensing automation that drops into one — typically the FLEX in our setup. This page explains, in plain language, what CRP does (precise F-18 vial dispensing, hands-out-of-cell), what it leaves to the host cell (shielding, Grade A environment, AERB licensing), and why the SYNT → FLEX + CRP stack is the Saxsons-supplied package for a modern Indian cyclotron radiopharmacy.

Where CRP sits

From the cyclotron to the patient — CRP is inside the FLEX

Step 1

Cyclotron

Particle accelerator makes the F-18

Step 2

SYNT

Automated chemistry turns it into FDG (or another PET tracer)

Step 3

FLEX + CRP

FLEX is the Grade A cell; CRP is the automation inside it

Step 4

Patient

Syringe leaves the cell, scanned within hours

Why this matters

Six things CRP delivers, explained simply

It's a module, not a hot cell

The automation that goes inside the shielded cell

Most things called "dispensing systems" come with their own shielded box. CRP is the opposite — it's the dispensing automation engineered to drop into a shielded hot cell you already have (or are buying alongside, like the FLEX). The host cell provides the shielding and the GMP environment; CRP brings the precision and the hands-out-of-cell workflow.

Based on: CRP product page — "compact dimensions, can be installed in any type of shielded laminar flow cell"

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Better than 1% precision

Volume deviation guaranteed under 1%

Patient dose accuracy starts with how precisely the volume is dispensed. (the manufacturer )guarantees CRP volume / weight deviation stays under 1% of target. That's the precision floor a modern radiopharmacy expects from an automated unit-dose bench.

Based on: CRP product page — "deviation from the target volume (weight) guaranteed to be less than 1%"

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Open and closed vials

Both vial workflows in one module

CRP Compact dispenses open vials (with rubber stopper + crimped aluminum-ring cap) and adds closed-vial via septum piercing as an option. CRP Compact plus does open-vial dispensing with either crimped or push-fit capping. The same module handles the F-18 unit-dose workflow shapes you'll meet day-to-day.

Based on: CRP product page — Compact and Compact plus variant descriptions

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Annex 1 compliant

Designed for sterile-conditions dispensing

The European pharmaceutical rules require unit-dose dispensing of sterile injectables to happen under aseptic conditions. CRP is positioned by (the manufacturer )as compliant with EU GMP Annex 1, the sterile-medicines rulebook (revised 2022). The host cell provides the Grade A environment; CRP runs the dispensing process inside it.

Based on: CRP product page — "compliant with EU GMP Annex 1 regulations"

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100 units worldwide

Not a first-of-its-kind risk

(the manufacturer )publishes a 100-units-installed install base for CRP. For an Indian cyclotron site evaluating dispensing automation, that's a meaningful reference base — the device exists, it ships, it works in clinical practice.

Based on: CRP product page — "100 CRP installed around the world"

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Pairs with FLEX

One manufacturer-supplied stack: SYNT → FLEX + CRP → patient

SYNT is where the chemistry happens; FLEX is the Grade A shielded cell where unit doses are drawn; CRP is the automation inside FLEX that actually does the dispensing. Buying all three as a the manufacturer stack means one calibration chain, one teleassistance contract, and one consistent audit trail across the cyclotron radiopharmacy.

Based on: SYNT + FLEX + CRP product pages

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CRP at a glance

< 1%

Volume deviation

(the manufacturer )guaranteed precision

100+

Units worldwide

manufacturer-published install base

Annex 1

EU GMP framework

Sterile-conditions compliant

F-18

India primary use

FDG unit-dose dispensing

Scope of this page

CRP is a dispensing module, not a hot cell. Lead shielding, Grade A environment and AERB licensing all sit with the host cell (typically the FLEX in a Saxsons-supplied Indian setup). The F-18 primary-use focus is Saxsons-supplied market reality — the CRP public page uses generic "radiopharmaceutical" language and does not name specific isotopes. The "compliant with EU GMP Annex 1" claim is Tema\'s marketing language; CRP is the automation that supports an Annex 1 workflow, but certification of the radiopharmacy programme is the operator\'s responsibility.