OUR FACILITY

R&D Laboratory

The GMPriority Pharma state-of-the-art liposome research and development laboratory is at the forefront of innovation in the field of lipid-based delivery systems.

Equipped with the latest technology and driven by a team of world-class scientists, we specialise in the design, characterisation, and production of advanced liposomal formulations.

Our commitment to excellence and unbeaten formulation stability ensures that we provide unparalleled services to our clients, from initial concept to final product.

Our Laboratory Equipment and Technologies

High-Performance Liquid Chromatography (HPLC)
Dynamic Light Scattering (DLS)
Transmission Electron Microscopy (TEM)
Ultracentrifugation System
Zetasizing
Stability Chamber

Our Advanced Capabilities and Expertise

Technology

Dynamic Light Scattering

Accurate measurement of particle size distribution, zeta potential, and stability of liposomal formulations

High-Performance Liquid Chromatography

Precise quantification and analysis of liposomal components and encapsulated actives.

Transmission Electron Microscopy

High-resolution imaging for detailed visualisation of liposome morphology and size.

Pioneering. Innovative.
Our Capabilities.

Formulation Development

Our team excels in the design and optimisation of liposomal formulations tailored to specific therapeutic needs. We utilise our unrivalled experience to achieve optimal encapsulation efficiency, release profiles, and targeting capabilities.

Analytical Characterisation

We offer a suite of analytical services to characterise the physicochemical properties of liposomes, including size, charge, morphology, and encapsulation efficiency. Our robust analytical techniques ensure reproducibility and quality control at every stage of development.

Scale-Up and Manufacturing

We provide seamless scale-up from lab-scale to pilot and full-scale production. Our manufacturing processes adhere to stringent regulatory standards, ensuring high-quality, reproducible liposomal products.

Class 7 Cleanroom

A Class 7 cleanroom, classified under the ISO standard, is a controlled environment with stringent contamination control protocols. It is designed to maintain low levels of particulates such as dust, airborne organisms, or vaporised particles, making it ideal for sensitive research and manufacturing processes, including those involving liposomal formulations.

Class 7 Cleanroom - Key Features

Air Quality and Filtration

HEPA Filtration:
High-Efficiency Particulate Air (HEPA) filters:
Essential for removing 99.97% of particles ≥0.3 microns from the air.

Air Changes Per Hour (ACH):
Class 7 cleanrooms typically achieve 30-60 air changes per hour to maintain air purity.

Positive Pressure:
Maintained to prevent infiltration of contaminants from adjacent areas with lower cleanliness standards.

Cleanroom Design and Layout

Material and Surface Selection:
Smooth, Non-Porous Surfaces:

To minimise particle accumulation and facilitate easy cleaning.
Low Outgassing Materials:
Used to prevent contamination from the materials themselves.
Laminar Airflow Systems:
Unidirectional Flow:
Ensures that air moves in a single direction, reducing turbulence and preventing particle settlement.

Airlocks and Gowning Areas:
Airlocks:
Prevent cross-contamination during entry and exit.
Gowning Procedures:
Strict protocols for donning cleanroom garments to minimise introduction of contaminants.

Documentation and Compliance

Standard Operating Procedures (SOPs):
Detailed Protocols:
Comprehensive documentation for all cleanroom operations and maintenance procedures.

Regulatory Compliance:
ISO Standards:
Adherence to ISO standards for cleanroom classification.
Validation and Certification:
Regular validation and certification to ensure compliance with regulatory requirements.

Our UK facility is dedicated to pushing the boundaries of lipid-based compound delivery. By combining cutting-edge equipment, expert knowledge, and a commitment to scientific excellence, we deliver innovative solutions that meet the highest standards of quality and efficacy.

OUR FACILITY