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Butterworth Laboratories Ltd.

Logo Butterworth Laboratories Ltd.
  • GLP services
  • Human Medicines
  • Europe, Worldwide

Providing excellence in  contract analytical chemistry through the skills, expertise, knowledge and dedication of our staff. With nearly 40 years experience, our company remains a fully independent UK contract analytical service providing QC testing, method development, method validation and stability services to the pharmaceutical, medical device and chemical industries. Regular inspections by the MHRA, UKAS and FDA ensures that the service provided is of the highest levels of quality. More »


Logo Biomapas
  • Clinical development and testing, clinical CRO
  • Human Medicines
  • Europe

Biomapas is a privately owned contract research organization (CRO), established in 2001. We have the capabilities of conducting Phase I-IV clinical trials including bioequivalence (PK/PD) studies for the pharmaceutical and biotechnology industries as shown by our continuing success.   Specialities: Clinical trial management and monitoring, regulatory affairs, pharmacovigilance. Geographic coverage:  Baltic countries (Lithuania, Latvia, Estonia) and Belarus. Experience in different therapeutic areas: We have a solid over 11 years and over 100 clinical trials experience in numerous therapeutic fields such as, but not limited to, cardiovascular (17% of all our studies), psychiatry (17% of all our studies), oncology (13% of all our studies), endocrinology (8% of all our studies), rheumatology (6% of all our studies). Investigators database: We personally know the key opinion leaders and overall we have investigators database with over 800 investigators. GCP trainings for investigators: We are CA authorised GCP trainers in Lithuania and we have already trained over 400 investigators. Excellent recruitment: The Baltic States are exclusively high recruitment countries. Belarus has a big pool of treatment naïve patients. Our achievement - 25% of our studies exceeded the target recruitment by 1.5 since year 2008. Personnel/CRAs:  Clinical research professionals with medical and pharmaceutical backgrounds, regular trainings, multilingual skills, average of over 3 years’ experience in clinical research field, low staff turnover (average staff turnover less than 10% over the last three years). Quality: Our quality is supervised by our internal Quality Management System which is ISO 9001 certified. Multidisciplinary team: State of the art solutions from early phase research all the way up to final product registration. Clinical Operations (clinical trials management and monitoring) department along with Regulatory Affairs and Pharmacovigilance departments creates solid multidisciplinary team. Feedback from customers (Sponsors): We are committed to customer service and satisfaction. Our customer survey shows that 93% of our customers evaluate our services quality as excellent/very good. More »


Logo Cromsource
  • Clinical development and testing, clinical CRO
  • Biopharmaceuticals
  • Europe, North America

CROMSOURCE is an ISO-certified international provider of outsourced services to the pharmaceutical, biotechnology and medical device industries, specialized in clinical development and staffing solutions.                                                                                     A well-established full-service CRO, CROMSOURCE is unique in offering an end-to-end guarantee covering trial timelines, enrolment and contract price. This guarantees our clients that their trials are delivered on time and within the contract price with no CRO initiated change orders. CROMSOURCE supports the full spectrum of clinical development via our Pharmaceutical, Medical Device, and Staffing Solutions divisions. More »

Minerva Scientific Ltd.

Logo Minerva Scientific Ltd.
  • Analytical laboratory and testing services
  • Human Medicines
  • Europe, North America, Australia & New Zealand

Established in 2001, we are a privately owned, contract testing laboratory based in Derbyshire, UK.  We specialise in the high-tech analysis of food, feeds, pharmaceuticals & veterinary products.  Our policy is to provide a "gold" standard testing and consultancy service to the Food and Pharmaceutical industries.  Minerva's modern facility is GMP compliant and accredited to ISO 17025 (UKAS).  Find out more at     More »


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Provence Technologies

Logo Provence Technologies
  • Pre-clinical development and testing, pre-clinical CRO
  • Biopharmaceuticals
  • Europe

Provence Technologies is a Contract Research Organization (CRO) providing fine organic chemistry solutions to pharmaceutical, biopharmaceutical, agrochemical and cosmetic industries. Our goal is to match our client’s requirements and keep on building a reputation that is synonymous with reactivity, efficiency, quality and reliability. Our strategy is aimed at becoming our client’s preferred partner for any issue dealing with fine organic chemistry. Provence Technologies was created in 1998 and is headquartered in Marseille. More »

Fujifilm Diosynth Biotechnologies

Logo Fujifilm Diosynth Biotechnologies
  • Contract manufacturing, filling and packaging
  • Human Medicines
  • Europe, North America, South America, Asia, Australia & New Zealand, Middle East, Africa, Worldwide

Fujifilm Diosynth Biotechnologies is an industry leading Biologics Contract Development and Manufacturing Organisation with locations in Billingham,United KingdomandResearch Triangle Park, North Carolina, USA.  Fujifilm Diosynth Biotechnologies has extensive experience in the development and manufacture of recombinant proteins, vaccines, monoclonal antibodies, among other large molecules, expressed in a wide array of microbial, mammalian, and insect systems.  We offer a comprehensive list of services from cell line and strain development, including its proprietary pAVEway™ and CHO cell line systems to process development, analytical development, clinical and commercial manufacturing.  Both sites are FDA-approved for the production of commercial products.  More »

Keyrus Biopharma - Keyrus group

Logo Keyrus Biopharma - Keyrus group
  • GCP audit services
  • Human Medicines
  • Europe, Middle East

Founded in 1998, our company, a European CRO (Contract Research Organisation) is a major player in clinical research, with 250 members located in France, Belgium, Lebanon and Tunisia. Capitalising on a solid experience in clinical research and a lasting relationship with its clients, our company focuses its development strategy on innovation and creativity to offer high standard solutions to its clients. From pharmaceutical industries to nutrition, cosmetics and biotechnology Based on its expertise gained over more than 15 years in clinical research, we have been able to meet the needs of clients in nutrition and cosmetic domains and to develop partnerships with the biotechnology industry. This diversity of experience and the know-how of our company result from a close collaboration based on innovation and a customer focused orientation. It is enhanced by the dedication of team members to our strategy based on expertise and skills development. As a result, we offer a wide range of solutions and services using the proficiency of its team and the command of the latest technologies (Oracle® Clinical, e-CRF, SAP BusinessObjects®, SAS®, etc) As a specialist in your area, we efficiently assist you in your projects: whatever their specificity in a more and more innovative environment in a tighter regulatory setting we benefit from the Research Tax Credit agreement (“Credit Impôt Recherche”) More »


Logo Storkbio
  • Formulation development and drug delivery
  • Biopharmaceuticals
  • Europe, Worldwide

Storkbio offers custom peptide synthesis, polyclonal and monoclonal antibody production. We help you to untwist your 3D-like puzzles related to peptide and antibody tasks and provide a custom solution from start to end. Storkbio, as an Estonian biotechnology company integrates existing productions resources in Estonia and so teams up the very specific knowledge of different biology and chemistry areas. People, involved in production, have over 15 years of experience and are specialists of their own area. This ensures quality at every production step, which brings satisfaction to our customers. More »

Tianjin International Joint Academy of Biotechnology & Medicine

Logo Tianjin International Joint Academy of Biotechnology & Medicine
  • Academic collaboration
  • Human Medicines
  • Europe, Asia, Worldwide

China needs to position itself as a global top player in biomedical innovation and industrialization , to boost the biomedical sector and to promote the development and opening-up of the Tianjin Binhai New Area. Four Ministries and One Municipal Government, namely, the Ministry of Science and Technology, the Ministry of Commerce, the Ministry of Health, the State Food and Drug Administration, and Tianjin Municipality, shed light on the Binhai New Area for being and established BioMed Zone. At the heart of the zone is the iconic 340-plus-mu TJAB, located at No. 220 Dongting Road, TEDA. Blessed with an investment a generous 1.1 billion Yuan, this institute dreams big, with a construction area of 350,000 square meters on its blueprints. This first project at TJAB, the 70,000-square-meter building, has been ready to serve since June 2009. Equipped with an abundant and diverse array of state-of-the-art devices in each of the eleven technical platforms for R&D of new pharmaceuticals, TJAB is proud to cater to R&D teams. Up till now, TJAB has been home to more than 104 R&D teams. More »


Logo Fluofarma
  • Pharmaceutical process development and validation
  • Human Medicines
  • Europe

Fluofarma joins drug discovery projects to bring tailored solutions in cell biology and high-content analysis. Specialized in assay design, the French preclinical CRO develops and performs cell-based assays and quantifies biomarkers in blood and tissues using different high-content imaging and flow cytometry technologies. More »

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