PharmiWeb.com - Global Pharma News & Resources

Company Directory

PharmiWeb's Pharma Company Directory is a comprehensive and searchable listing of organisations within the Pharma, Biotech & Life Sciences sector. Use it to find partner organisations, suppliers, or even a company to work for!

As an organisation, a basic listing is FREE, and can raise your profile in the industry, making you visible to thousands of monthly site visitors.

To add your organisation to the directory, simply register as a contributor and add your organisation's details. You can also upgrade to a premium listing for only £500/year, this offers even greater scope for added content (more photos, more links, more copy), and even more exposure.

Note that we only accept contributions relating to the Pharma industry and that it will typically take 2 working days to approve (or otherwise) your details. Once approved, you will also be able to contribute press releases and event details to our site.

Create a free account to list your company for free!

At Cunesoft we provide intelligent software for regulatory data management to the Life Sciences Industry, delivered as Software as a Service (SaaS). Our customers benefit from process automation combined with compliant document, data and submission management. Our innovative technologies include leading edge machine learning algorithms with ready-to-use document data mining and data extraction solutions that can result in ROI’s of 12 months or less. And everything we do is supported by our global team 100% focused on client satisfaction and user happiness.
We are a virtual CRO, purpose-built to execute the unique clinical services required for decentralized clinical trials. Our experienced team of principal investigators and study team members work directly with sponsors to develop a protocol that supports a decentralized trial.
We are pioneering the development of a completely new class of drugs based on the messenger RNA (mRNA) molecule. The basic principle is the use of this molecule as a data carrier for information, with the help of which the body can produce its own active ingredients for fighting various diseases.
Curia is a global contract research, development and manufacturing organization (CDMO), offering products and services across the drug development spectrum to help our partners turn their ideas into real-world impact. We partner closely with pharmaceutical and biotechnology companies to boost business performance and improve patients’ lives.
We are dedicated to fundamentally changing the mental healthcare experience for those affected by mental illness, and their loved ones, through delivering powerful and effective new psychedelic-based therapies that are accessible to all.
Founded in 2017 by Flagship Pioneering, Cygnal Therapeutics is the first company to build a platform to develop drugs in the field of exoneural biology. Exoneural biology is broadly implicated in human health and disease. We are creating new medicines across multiple therapeutic areas, starting with cancer and inflammatory diseases.
Cyprotex specialises in in vitro and in silico ADME-Tox services. This includes in vitro ADME screening to support discovery projects, regulatory in vitro ADME and DDI studies during preclinical and clinical development, specialist mechanistic in vitro human and animal toxicity models (e.g. 3D models and MEA electrophysiology) and PBPK/QSAR modelling expertise.
The clinical development of drugs and devices is crucial for human welfare. Our mission is to improve success rates in this endeavor. We do this by improving the design and implementation of clinical trials through the innovative application of stat
Since 2007, DAVA has utilized a vast network of oncologists to provide innovative solutions and services to the pharmaceutical industry through each step on the drug development process. We strive to advance oncology patient care through support of our life science partners at each obstacle they face.
Pharmacovigilance Services in UK ensure drug safety, monitoring adverse effects post-market, while Regulatory Services in UK govern the authorization and compliance of therapeutic goods, upholding healthcare standards.
Adapting multiple skils and services, DFC Tank Pressure Vessel Manufacturer Co.,Ltd has earned its reputation in the line of pressure vesssels production for her quality, price,responsilbe staffs and competitive engineers since 1984.
Building on our heritage in pharmaceutical grade lactose, DFE Pharma provides a wide range of excipient products and services for oral solid dose and dry powder inhalation formulations, and we do it on a global basis. We live up to our values to deliver the best, today, tomorrow, always.
To keep you at the forefront, DIA offers face-to-face, and online courses (including eLearning programs), certificate programs, and can provide learning for groups at your organization. We also offer live and on-demand solution provider webinars.
DNA Script was created to revolutionize DNA write with enzymes. Our core R&D efforts have produced innovations in enzyme engineering, surface and nucleotide chemistries, and instrumentation. The integration of these innovations has resulted in SYNTAXTM, the world’s first benchtop DNA printer powered by enzymatic technology.
DOCS provides global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.
DOCS provides global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.
DP Clinical, Inc. is a privately held Contract Research Organization (CRO) specializing in dermatology, infectious disease/vaccine, neuroscience (including spinal cord injury), oncology, and ophthalmology, Phase I-III clinical programs. DP Clinical provides a full complement of clinical trial services to pharmaceutical, biotech, and medical device companies including trial management, monitoring, data management, biostatistics, regulatory, safety monitoring and reporting, and medical writing.