Laboratory and Analytical Services

Our state-of-the-art analytical testing laboratories support drug substance (API) and drug product analytics from early clinical development through to commercial release. Employing over 700 highly skilled analysts across the UK, Europe and the US, we operate in GMP-approved environments and pr...

Comprehensive GI Transit Simulation using AMP™

Using our versatile AMP™ dissolution platform, we accurately replicate both fasted and fed states by simulating the full complexity of gastrointestinal transit:

• Biorelevant Media: Customized media including hydrogen carbonate buffers, ...

Getting 3D data for your research is easy: just send us your sample, and we handle the rest. No equipment, expertise, or special preparation is needed. Choose between two options: a small 5 mm tissue core, scanned at a resolution of 2.5 µm for detailed views (punched out by you or by our team), or your who...

To meet your unique pharma and biopharma outsourcing needs, Intertek delivers quality and safety through pharmaceutical contract laboratory services, regulatory support, and supply chain assurance. We bring quality and safety to life!

With our pharmaceutical experts working with you at ...

Lambda provides regulated bioanalytical support for large molecules, biologics and biosimilars across clinical development. Capabilities include large-molecule PK analysis, anti-drug antibody assessment, neutralizing antibody testing, pharmacodynamic biomarkers, functional bioassays, immunogenicity assessm...

ESTEVE CDMO provides integrated, phase-appropriate API and HPAPI development services for complex small molecules, from early route design and reaction screening to process optimization, scale-up and pre-validation. 
Our global R&D teams combine process chemistry, analytical development, proc...

Over 400 developed recipes, 
including over 30 medical devices in various classes and indications,
in 20 pharmaceutical forms - 
everything starts in the Gofarm's R&D Laboratory.



In Gofarm's R&D Laboratory our and our clients' ideas take real shapes...

A correct formulation means greater stability of the active ingredient and provides protection against the stress suffered during the lyophilization process itself.

The selection of the appropriate excipients is really important in the development of a freeze-dried product.

Pharmaceutical reference standards are essential for ensuring the quality, safety and efficacy of pharmaceuticals. These meticulously characterized materials serve as benchmarks for analytical testing, enabling manufacturers to verify the identity, purity and potency of active pharmaceutical ingredients (A...

TP&C provides tailored formulation development services for pharmaceutical, OTC and dermo-cosmetic products, adapting each project to target performance, regulatory needs and manufacturing constraints. From concept to scale-up, the R&D teams support partners with formulation optimization, stability...

As part of our QP services and our pharmaceutical consulting, we offer you comprehensive monitoring and assurance of product quality in accordance with the Good Manufacturing Practice (GMP) guidelines and the specific requirements of § 13 AMG. We provide the following services:
• Setting up your Q...

Ph. Eur. reference standards (RSs) are essential for carrying out the quality control tests described in the Ph. Eur. and comprise chemical reference substances (CRSs), herbal reference standards (HRSs) and biological reference preparations (BRPs). 

https://store.edqm.eu/index.html

At Sofgen Pharma, we go beyond traditional softgels, offering solutions ranging from single-unit dosage forms to multiple delivery systems within a single dose.

Softgels are an effective oral delivery system, especially for active ingredients with low solubility and/or permeability (BCS Classes ...

This type of calibration activities are performed through Altiorlab, QSGroup's ISO 17025:2018 ILAC MRA certified laboratory. QSGroup is the first and only Company in the world to offer ISO 17025:2018 ILAC MRA certification on TOC.

The determination of the T.O.C. (Total Organic Carbon) in ...

As a proven leader in the production of biologics and small molecules from first-in-human (FIH) trials to commercial-scale manufacturing, we can help you advance to market quicker. With many format and formulation choices available including lyophilized, we can manufacture the right for...

ZebraSci – a BD Company – provides expert combination product testing and advisory services, supporting customers from concept to commercialization to ensure performance, compliance, and patient safety.
How can we partner with you to serve your combination product development needs?zebrasci.comsa...

Catalyx employees are deployed onto a client site to integrate into the client’s team(s) to supplement their internal headcount, these embedded resources work under the client’s supervision for specific roles.

-  Managed, Flexible & Scalable Solutions 
-  GMP Expertise &a...

Alcami offers fully-integrated analytical method development, method validation and testing solutions for raw materials, API/BDS and Drug Product.Built on a foundation of comprehensive analytical services for pharmaceuticals including biologics, our advanced laboratories and experienced scientist...

• API / GMP Manufacturing • Rapid Process Development, Flawless Upscaling, and Economy of Scale-Production  • Simulated-Moving Bed (SMB) Chromatography  • Heterocyclic, Hazardous and Malodorous Chemistries • Organometallic and Cryogenic Chemistry • Transition-Metal Catalysis • High-Pressur...

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Merieux NutriSciences has developed various strategies and complementary approaches for the identification of foreign visible and subvisible particles, thanks to sophisticated instrumentation combined with a pool of experts in different fields.