Pharmaceutical Industry Consultancy, Testing and Laboratory Services

At Lucideon, we bring world-leading materials science and analytical capabilities combined with a consultative approach to the pharmaceutical sector, solving complex product and process challenges. We work with drug developers, manufacturers, CROs, and CDMOs to accelerate innovation and strengthen regulatory confidence.

With GMP and ISO 17025 accredited laboratories in the UK and a multidisciplinary team of scientists, engineers, and regulatory specialists around the globe, we help pharmaceutical organisations de-risk development, enhance product performance, and bring high-quality therapies to market faster and more efficiently.

Lucideon's pharmaceutical solutions

We provide comprehensive analytical support across the full product lifecycle, from early R&D development through to routine quality control testing. Alongside compliance with global regulatory expectations, these services help ensure product quality and consistency.

Our services include:

Stability studies – assessment of how products and materials change over time under controlled conditions, generating the data needed to optimise formulations and support regulatory shelf‑life requirements
Chemical and elemental characterisation – analysis of chemical composition and elemental profiles to confirm material identity, purity, and quality to diagnose issues such as impurities or degradation
Particle size, morphology, and distribution analysis - particle size, shape, and distribution analysis to understand flow, dissolution, stability, and overall product performance
Surface analysis - surface chemistry and structure investigation to identify contaminants, investigate performance issues, and support material selection and product optimisation
Cell biology - Lucideon's in vitro cell biology testing laboratory offers a range of investigative and analytical solutions to support our customers' research & development and discovery through cytotoxicity testing, equivalence studies, and more
Microbiological testing – we provide sterility, bioburden, endotoxin testing, and antimicrobial effectiveness testing to ensure products meet safety standards throughout development and manufacturing

Environmental monitoring – assessment and monitoring of microbial and particulate levels in cleanroom environments to maintain GMP control and safeguard product quality
Materials & formulation expertise - understand and optimise the behaviour of APIs, excipients, and finished dosage forms. We offer solid‑state analysis as well as support for small‑molecule formulations and advanced delivery systems and troubleshooting of formulation stability
Regulatory & compliance testing - we design and execute testing programmes aligned with FDA, EMA, and ICH requirements to support submissions and risk assessments, as well as ensuring ongoing compliance. Including biocompatibility evaluations and extractables and leachables studies for packaging and devices
Failure & contamination analysis - our rapid‑response investigation teams help identify root causes and restore control. Our independent, evidence‑driven approach helps clients resolve issues quickly and maintain product integrity. We investigate chemical, particulate, fibre, and biological contaminants

Areas of application

Our materials expertise and analytical capabilities support a broad range of pharmaceutical products and processes, including:

Prescription medicines
Over‑the‑counter (OTC) products
Biologics and advanced therapies
Radiopharmaceuticals
Topical and transdermal products
Inhalation medicines
Injectable and parenteral products

Whether you're developing a new therapy, troubleshooting a manufacturing challenge, or preparing for regulatory submission, Lucideon provides the scientific foundation and technical clarity needed to move forward with confidence.

Collaborative R&D support

We partner with organisations on projects that push the boundaries of drug delivery and manufacturing. We act as an extension of your team, providing the scientific insight and technical capability needed to accelerate progress.

Our R&D support includes: