Corporate Members

CONVIDIA clinical research ConsulTech GmbH LUMIS International Dr. Notghi Contract Research Mares Sacura biosafety4u SCC GmbH Richmond Pharmacology

Conelis e. V. recognizes with gratitude the support given by its Corporate Members helping us to improve consulting in the Life Sciences Industry.

Sacura is a full service CRO experienced in 120 clinical trials and 70 indications, guarantees high quality services and transparency of work.

  • Clinical study set-up, management and monitoring
  • Regulatory support
  • Data and document managements

LUMIS International is specialized to provide start up and market entry services for small biopharmaceutical companies conducting clinical trials in Europe.

  • Legal Representation in Europe for Clinical trials for Non-European companies
  • Vendor selection and vendor management
  • Medical and scientific support to meet European requirements

CONVIDIA clinical research GmbH is a full-service employee-owned CRO with 15 years extensive working experience in a wide variety of indications including stem cell studies.

  • Clinical studies Phase II-IV and non-interventional studies (set-up, project management, monitoring)
  • Quality management (SOP writing, Auditing)
  • Medical Writing

Contact person:

Stefan Siegmund

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Richmond Pharmacology is an early phase CRO with a specialist focus on Adaptive, Cardiac Safety, Japanese and Patient Studies.

  • MHRA accredited hospital based trials unit
  • Full clinical trial service under-one-roof
  • Longstanding success led by acclaimed team of experts

We advise companies and research institutions on possibilities for financing research and development projects with the help of grants. We have specialized in the areas of biotechnology, pharmaceuticals, medical and environmental technology and sciences as well as IT services for the life sciences sector.


  • funding check
  • development of an individual funding strategy
  • elaboration of proposals
  • proposal management, administrative support
  • financial planning
  • project management, administrative service
  • dissemination and exploitation of results GmbH is a service provider supervising genetic engineering facilities in all federal states of Germany in compliance with the German Genetic Engineering Act. We provide services throughout the complete life cycle of a genetic engineering laboratory: Design Phase – Project Phase – Operational Phase – Retirement Phase. We help you setting up a lab facility in compliance to Good Laboratory Practice (GLP) and the Good Clinical Laboratory Practice (GCLP) requirements.

flyer biosafety4u
Flyer (PDF)

SCC – Scientific Consulting Company - is a privately owned and independent scientific and regulatory consulting company and provides support in various fields such as agrochemicals, biocides, chemicals, consumer products, cosmetics, medical devices and pharmaceuticals.

For pharmaceuticals, SCC is specialized in

  • Environmental risk assessments (ERA, Module 1.6.1)
  • Persistence, bioaccumulation and toxicity (PBT) assessment
  • Derivation of the environmental quality standards (EQS)
  • Derivation of the German water hazard classes (Wassergefährdungsklassen, WGK)
  • Study planning and study monitoring of all kind of studies required in this context (ecotoxicology, toxicology, environmental fate and behaviour and physical chemistry)

Dr. Notghi Contract Research GmbH is a full service CRO in Berlin. Our focus is on high quality with fair prices, quicker results and full customer satisfaction. With 20 years of experience we offer services for pharmaceuticals, consumer healthcare/OTC, and Medical devices.

  • Full Clinical Trials Services: DM, Monitoring, SAS
  • Pharmacovigilance
  • Medical Writing and Regulatory, MDR and Clinical Evaluation,
  • Training, Academy and Workshops

Mares develops advanced-therapy medicinal products (ATMPs) such cell & gene therapy as well as tissue engineered products and provides hands-on solutions for each stage of the value chain, such as:

  • Preclinical Test, Process Development and Manufacturing Authorization
  • Clinical Trial Dossiers and Clinical Trials
  • Marketing Authorization and Upscaling, GMP-Audits

Beyond ATMPs, we search for and identify technologies for various chemical applications.

Image brochure Mares
Image brochure (PDF)