Contract Research Organisations (CROs) (Services)

FForce helps sales teams manage leads, automate tasks, and track performance to close deals faster and grow revenue.

Modules:
• Sales Force Automation: Automates lead management, CRM tasks, and sales tracking.

• Digital Engagement Platform: Connects with customers across chan...

Our R&D Services are categorized into 8 streams: • Material Science Services

• Metal and Organic Scavenging Screening Services

• Organic Synthesis Services

• Catalysis Services

• Process Services

• Chromatography and Purification Services

• Method D...

Recipharm offer formulation development services for all dosage forms. We develop everything from simple formulations for early studies to more complex formulations suited for commercialisation.

ProPharma's validation professionals leverage the latest risk-based Computer System Validation (CSV) and Computer Software Assurance (CSA) techniques to ensure that our clients' systems are ready for inspections from the FDA, EMA, MHRA, and other regulatory agencies. Our consultants have extensive experien...

• Sterility Testing • Quality Control Release • Bioburden Testing • Method Suitability • Microbial Identification - MALDI-TOF • Bacterial Endotoxin Testing • Cytotoxicity • Environmental Monitoring • Biological Indicator Enumeration

With 55+ years of experience, our expert teams develop 1,000+ analytical methods and validate 250+ methods annually. Drawing upon an extensive range of analytical technology, combined with a wealth of analytical knowledge, we can add real value to your drug development and commercialisation programs....

Experienced cell-based neutralizing antibody assay capabilities. Our experts, at our GLP/GCP compliant laboratory, evaluate each therapeutic, conduct tailored assay development and ensure that each assay is optimized to suitably determine the presence of NAb with maximum possible level of drug toleran...

The TIM-2, as part of the SurroGUT™ platform, is the dynamic in vitro model of the large intestine. The lower GI model, with its anaerobic compartment containing highly metabolic active intestinal microbiota, precisely mimics the physiological conditions of the colon in vivo. TIM-2 can simulate the pr...

Navigate the regulatory landscape and efficiently drive strategic decisions with Cortellis Regulatory Intelligence. Get full and timely coverage of global health authority requirements on healthcare products such as drugs, biologics, medical devices and IVDs, and access exclusive expert reports for both in...

We offer a full range of studies and bioanalytical services, providing powerful tools and rigorous solutions for preclinical drug development of therapeutic candidates, advance lead compounds towards first-in- human trials, and support for ongoing clinical development

1) Physico-Chemical Testing of Raw Material & Finished Medical Devices2) Biocompatibility Testing of Medical Devices(As per ISO 10993-1:2018)
3) Biological Testing of Raw Material of Plastic, Rubber,Silicone, Polymers, etc.(As per IP / BP / EP / JP / USP)
4) Microbiological Testing Services ...

We support our clients from early-stage research and preclinical phase to and beyond market approval by providing comprehensive development services, including 

• Developability assessment • Pre-formulation screening • Formulation development • Lyophilization process development • Forced d...

KBI Biopharma offers a broad range of cGMP biologics manufacturing services to biopharmaceutical companies worldwide. Our capabilities include reliable manufacturing for preclinical and clinical supply.

KBI’s experienced team produces high-quality therapeutics and vaccines thro...

Conscio's in-house clinical Unit has been operating since 2007, with more than 600 BA/BE/PK studies completed and proprietary of over 270 validated bioanalytical methods. Equipped with a 60-bed on-site clinical unit in Prague and a recently opened 36-bed unit in Ostrava, we provide comprehensive services w...

Huayi Pharmaceuticals offers an integrated service for product development with our partners Weida Clinical Research and Velocyte Analytical Technology for your bioequivalence needs in China. Through these close strategic partnerships, we are able to offer a one-stop service which allows pharmaceutical dev...

Delivering rapid bioanalytical data in discovery – preclinical – clinical. Bioanalysis is a critical step in the drug development process.  At Quotient, we are experts in the development, validation, and application of bioanalytical assays.  
Our dedicated team of bioanalytical chemists...

A small and powerful manually operated tablet laser drilling and writing machine for products of all shapes and sizes. Accommodates tablets, capsules or soft gels and manages multiple recipes. From laser marking soft gels to laser drilling tablets for controlled release, it delivers consistent, high qualit...

Equilab International is the leading Bioavailability/Bioequivalence (BA/BE) & Clinical Research centre in Southeast Asia and became the first BA/BE centre recognized by UK-MHRA in Southeast Asia and we are also the first BA/BE centre certified by NPRA Malaysia in outside Malaysia.

S...

Ardena offers services under brand pharmavize which includes drug product manufacturing service. It can manufacture various dosage forms, including: solutions and (nano-)suspensions, powder and granule filled capsules, semi-solid and, liquid filled capsules, topical products, tablets, modified-release prod...

Contract Research Laboratory. Analytical Services (physicochemical analysis, microbiological analysis and stability studies) and EU Import Lab.