PURE Innovation Biotech
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Biomanufacturing

GMP‑minded process development, scale‑up and QC to bridge research and production.

Biomanufacturing

Overview

We combine automation, computational design, and rigorous documentation to shorten research cycles and increase reproducibility.

Quality

GxP‑aligned methods and change control ready for scale.

Security

Project data isolated with audited access.

Capabilities

Upstream Process Dev

Strain/cell line selection, media optimization, DoE.

Downstream Purification

Chromatography, filtration, and polishing strategies.

Analytics

LC‑MS, HPLC, ELISA; orthogonal characterization.

Formulation

Stability screening and stress testing.

Tech Transfer

CPP mapping, batch records, and training.

Supply & QC

Materials, specs, and release testing workflows.

Workflow

Assess & Plan
Gap analysis, CMC roadmap, risk register.
Scale‑up Studies
Bioreactors to pilot scale with PAT.
Purification Train
Yield/recovery optimization and impurity profiling.
Analytical Methods
Method development & qualification.
Stability & Formulation
Shelf‑life studies and container closure.
GMP Readiness
Validation plans, SOPs, and tech transfer.

Platforms & Equipment

Bioreactors

Ambr/small‑scale systems for rapid iteration.

Chromatography

FPLC/AKTA for scalable purification.

QC Lab

Compendial methods and documentation.

Contact

Get in touch

We’d love to hear about your program.

Email: pibbiotech@gmail.com
HQ: Flat 701, 11 Florinis Street, 7th Floor, 1065 Nicosia, Cyprus

Collaborations

Partner with us for discovery, diagnostics, or manufacturing.

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