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  • Contract manufacturing, filling and packaging
  • Human Medicines
  • Europe

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Ethical GmbH

Logo Ethical GmbH
  • Pharmaceutical process development and validation
  • Human Medicines
  • Europe, Worldwide

Ethical eAdjudication®  Clinical Endpoint Adjudication made simpler, effective & GxP compliant with a focused Cloud Software Service.  Ethical supports Endpoint Adjudication with a user-friendly professional software solution designed to ease the daily work of Adjudication Staff and Adjudication Committees (CEC). The software is GxP / 21 CFR part 11 validated and has been designed for flexibility and completeness. A set of Software APIs allows the direct integration and data transfer with practically any other eClinical solution for Medical Record collection and assembling.  Ethical is located in Basel Switzerland and it has been founded by GM Servizi an Italian company that contributed to hundred of Clinical Trials with the design & management of CTMS, EDC, Safety Databases, Patients' Registries and Endpoint Adjudication solutions in partnership with Pharma Companies or CROs.  More »

Charnley Nickols Associates Ltd.

Logo Charnley Nickols Associates Ltd.
  • GCP audit services
  • Human Medicines
  • Worldwide

We are an independent company, we provide practical, unbiased and targeted advice to achieve compliance and enhance quality. We have been successfully assisting companies worldwide for over 15 years and this is evidenced by our many long-term relationships with customers. We provide worldwide services in clinical research and pharmacovigilance. We work to current international and national regulatory standards and best practice. More »


Logo Histologix
  • GLP services
  • Human Medicines
  • Europe

HistologiX Ltd is a rapidly growing GLP accredited Contract Research Organisation (CRO) providing commercial services to the Pharmaceutical, Biotechnology and Academic/Healthcare industries in Histology, Immunohistochemistry (IHC), Human Tissue Procurement, Clinical Trials, Molecular Biology and Advisory Consultancy. The Company was formed in 2005 by individuals with extensive experience in regulatory and non-regulatory diagnostic and clinical histology as well as IHC. HistologiX has a suite of dedicated laboratories within BioCity a science incubator facility, based in Nottingham, UK. HistologiX is focused on providing timely and quality solutions for our clients in all aspects of their histological, IHC and human tissue requirements. We will continually work in close collaboration to achieve these aims. More »


  • GCP audit services
  • Human Medicines
  • Europe

SynapCon Ltd. is offering international clinical project management and clinical monitoring combined with IT services, consultancy and compliance services for SME´s of other branches as well. Latter includes analysis, implementation and monitoring of compliance structures, quality control and risk management. We have special expertise and experience with different orphan indications in our clinical services.     Compliance management for SME (KMU) : Analysis, implementation and monitoring of compliance structures, quality control and risk management Regulatory services: Submissions to EC/CA/local authorities and follow up, preparation and consultancy for inspections Clinical Services: Feasibility, site selection, contract negotiations, project management, monitoring Consultancy: IT systems and infrastructure, strategic planning Training and Education: Project and Risk Management, Clinical Research (SOP, ICH-GCP) More »


  • Service delivered in time, perfect pre-study feasibility

Genau and More

  • Pharmaceutical process development and validation
  • Biopharmaceuticals
  • Europe

Compliance services for life sciences   We work together to help you optimise your approach to regulatory compliance. Our compliance work assures that you always operate according to the latest regulations and standards, while our management work assures a focus on the relevant business processes. We provide you with accurate regulatory interpretations that will allow you to form and maintain a competitive advantage based on Long term inspection readiness Fast time to market Reduced compliance costs Our core competences consist of 4 interconnected compliance services for which we provide you with business methodologies, tools, approaches and best practices, these are: Project Management Gap Analysis Validation (IT and Process) Change Management More »


Logo CIS
  • GCP audit services
  • Human Medicines
  • Europe

CIS Clinical Investigation Support is a completely independent, internationally operating contract research organisation. CIS Clinical Investigation Support Pharmaforschung GmbH was founded in 1990. CIS offers consulting services in clinical research and development, in particular in areas of quality assurance. CIS has a documented broad international experience in West and East Europe, but also in non-European countries. The office is easy to reach either by car, train or flight connections, despite of being located in the center of the city. More »


Logo Makrocare
  • Pharmaceutical process development and validation
  • Human Medicines
  • Europe, North America, Asia, Worldwide

MakroCare is a world class drug development and commercialization partner for pharmaceutical, biotechnology and medical device industries. Our experience, programs and processes bring a new dimension to development strategy, regulatory, clinical research, market access/expansion allowing our clients to incorporate an information strategy into the design and management of their programs. MakroCare has operations and presence in US, UK, EU, and Asia. MakroCare is well positioned to meet the demands of the expanding product portfolio needs of our life sciences clients worldwide. We also understand the demands of an increasingly competitive market. More »

TMQA (Tower Mains Quality Assurance)

Logo TMQA (Tower Mains Quality Assurance)
  • GMP audit services
  • Human Medicines
  • Europe

TMQA provides worldwide audit, consultancy and training support in Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GVP), Medical Devices, ISO standards and non-regulated research. More »

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