We live and expand partnerships to connect, extend and augment competencies
We are experts for plastic. We develop and produce solutions for different industry branches including innovative housing solutions for the medical sector. Rely on 22 years expertise in product development with a focus on plastic and a unique manufacturing process for express injection molding prototypes.
We are a CRO offering research services to pharma/biotech companies and academic organizations. Our mission is to accelerate our partner’s research programs by developing and executing predictive and scalable assays to quantify the bioactivity of novel chemical and biological entities. Assay.Works builds on the 16-year legacy of a leading biopharma's HTS center where we provided assay, screening, and quantitative biology services for drug discovery programs across indications with high medical need.
Bellingswood MedTech is a consulting company for regulatory requirements of medical devices and drug combination products. With our multidisciplinary teams of highly qualified experts, we provide a wide range of regulatory and clinical expertise such as global registrations, clinical evaluations and biocompatibility assessments.
Matrix Requirements offers software solutions to help medical device manufacturers creating and maintaining the technical documentation needed for certification and audits. Our products help to reduce the effort and complexity involved in creating these, allowing to release medical devices faster, with less risk of delays due to incomplete or wrong documentation.
We specialize in the supply of comparator products and analytical samples for biosimilar development. Cost effective approaches and individual project solutions are our core business on a day to day basis. We source comparator products from almost anywhere in the world and have direct access to many innovators and approved supply sources.
MedTech Pharma e.V.
MedTech Pharma e.V. is the largest network for health care in Germany and Europe. The association promotes cooperations, facilitates contacts and provides news about trends and innovations for expert meetings, symposiums and professional trainings. About 550 member institutions from science, economy, clinical sector, and heath care area arise from Germany and 12 other countries. If you are interested in further informations, please look at www.medtech-pharma.de.
Sourcia is a full service CRO tailor-made for small to medium-sized companies. Sourcia is your highly experienced, flexible and independent partner in clinical development. While you are focusing on sciences, we are your partner in project management from pre-clinical till clinical, operational set-up and execution of your clinical development plan and potential support in G&A activities.”
Medical Device and Biopharma firms have gained an edge utilizing ZebraSci’s device development services and ISO 17025:2005 accredited COMBINATION PRODUCT testing lab and technologies. ZebraSci is comprised of cross functional teams that are passionate about developing and launching combination products. ZebraSci offers project management throughout the entire product life-cycle ensuring product is launched, on time, on budget, and in compliance with ISO 13485 and FDA 21 CFR 820.
BIOPHARMACEUTICALS ARE SPECIAL!
Key ingredients for successful development, approval and partnering are promising compounds, tailor made approaches and skilled people with an eye for the essential. We provide targeted solutions for the development and approval of your products and support your company and people to excel. This is our commitment to excellence.
RQon is a regulatory consultancy for medical devices and drug companies. We assist our clients in aspects of regulatory and quality from product development to product registration to attain market approval in ASIA, ASEAN, EU, US, and the Rest of the World. Our range of clients includes researchers, manufacturers and traders from both start-ups and MNCs. Additionally, ARQon provides training sessions for researchers, manufacturers and regulators.
Ascendo focuses on professional project management as well as targeted research, development and teaching. As a guarantor of success, ascendo would like to ensure that innovations are implemented professionally, so that studies, pilot projects and prototypes will later become products, systems and solutions which can be used permanently in daily operations. As an proven expert in the fields of quality-management and compliance (ISO, GxP, Part11, DSGVO / GDPR), ascendo operates as a valued partner for anteris.