CRO Services Products & Reviews

25

Explore the comprehensive range of services offered by Contract Research Organizations (CROs) to streamline drug development and clinical research. From preclinical studies to regulatory support and clinical trials, CROs provide expert solutions that help pharmaceutical and biotech companies bring products to market faster and more efficiently.

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Digital Pathology Services

The Niche CRO Group

HistologiX is a leading GLP/GCP accredited Contract Research Organisation based in the UK specialising in Histology, Immunohistochemistry (IHC) and Digital Pathology services. HistologiX works with a broad range of clients from big pharma to small and medium biotech companies worldwide. Our team of scientists have in excess of 120 years combined experience and a customer retention rate of 80%. 

5.0/5.0
|1 Review

CRO Services

Svar Life Science AB

Svar CRO Services provides direct value through an extensive toolbox of in-house products, scientific expertise, and end-to-end customizable solutions – everything to ensure the success of your drug development program.​

0.0/5.0
|0 Reviews
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Discovery CRO

Cresset

Cresset Discovery is a premier computational chemistry CRO with a proven track record delivering high impact drug discovery projects. From ideation to synthesis and biological results, their expert CADD scientists are the best at what they do. Working alongside you from the ground up, they apply the best in silico techniques, and give expert advice and guidance, to accelerate your assets through the pipeline.

0.0/5.0
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In vitro NASH Contract Research Services by CN Bio

CN Bio

CN Bio supports non-alcoholic steatohepatitis (NASH) therapeutic development via fast-track NASH Contract Research Services. NASH Services enable you to gain instant access to CN Bio’s expertise and one of the most advanced human in vitro models available. Submit lead candidates for screening and receive human translatable data for insightful preclinical candidate prioritization, clinical trial design and optimization.

0.0/5.0
|0 Reviews


QPS Global Regulatory Affairs Services

QPS

QPS Global Custom-Built Regulatory Services Can Transform Clinical Trials.  QPS Global Regulatory Affairs (GRA) service offerings focus on helping pharmaceutical, biotechnology, and medical device companies to develop custom-built research solutions that forge expedited regulatory pathways from discovery to global commercialization and onwards through product lifecycle support. 

0.0/5.0
|0 Reviews

QPS Clinical Phase I/IIa Development Services

QPS

Moving quickly and safely through Phase I/IIa trials is critical to successful drug development.  The QPS Phase I research facilities feature more than 550 beds across six strategically located facilities on three continents. QPS is well known for its success in first-in-human clinical trials. All Phase I sites are staffed by expert clinical pharmacology teams that routinely conduct hundreds of phase I/IIa studies annually. 

0.0/5.0
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QPS Clinical Phase II/IV Development Services

QPS

At QPS, we realize that in today’s late stage drug development space you face many challenges.  With our deep experience and broad global presence, QPS is in an excellent position to offer solutions to all of the above needs. With its site management & monitoring teams operating from 30 locations on three continents (Asia/Pacific, USA, and Europe), QPS has become a new strong player in Phase II/IV clinical research services. 

0.0/5.0
|0 Reviews