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Welcome to Breuer Consulting AB
Consultant in Clinical Pharmacology, and Clinical & Preclinical **** Development
LAP&P Consultants
LAP&P offers Pharmacometric Services during preclinical and clinical phases of **** Discovery and Development.
Japan Pharmaceutical Consulting Web Site
Japan Pharmaceutical Consulting is a service provided by PointPath.Biz, K. K. It provides consulting services in pharmaceutical development in Japan, by industry experienced experts. JPC help your clinical studies and regulatory submissions in Japan. Preclinical to clinical development, IND to NDA, regulatory consultations. CMC and Patent. Small molecules and biologic products.
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NeuroDeRisk | Neurotoxicity De-Risking in Preclinical **** Discovery
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Clinical Trial Experts
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Partners for Medical Writing - Trilogy Writing & Consulting GmbH - providing all necessary regulatory documentation in support of your clinical development.
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CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
CaRACS
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
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MC Toxicology Consulting supports **** development by designing tailored, product- and indication-specific non-clinical programs.
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MC TOXICON
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Regulatory Affairs Consultants (RAC) Netherlands provides RA services to the pharmaceutical/biotech industry on European **** Regulatory Procedures. Our services range from the pre-marketing authorisation application (MAA) phase to the post-MAA phase, including the application for reimbursement (in...
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Contract research organization specialized in seamless, end-to-end, early phase **** development, we act to get your most promising compounds into and through early phase clinical trials.
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Contract research organization specialized in seamless, end-to-end, early phase **** development, we act to get your most promising compounds into and through early phase clinical trials.
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Contract research organization specialized in seamless, end-to-end, early phase **** development, we act to get your most promising compounds into and through early phase clinical trials.
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Biotrial- Your partner in non-clinical research and clinical trials - Biotrial
Biotrial is specialized in early **** developement process . We provide our expertise in conducting preclinical and clinical studies for biotechs, midsize and large pharma companies
What else preclinconsulting.ch alternative websites
2nd Dermatology **** Development Europe 2021 | February 17-19 | Virtual Event
Discover new preclinical modelling solutions, debate the optimal formulation strategy, define your clinical development plan, appreciate the regulatory considerations and evaluate different commercialisation routes. Learn more.
Prague Clinical Services
Our experienced team provides a complete solution for clinical research projects in all phases of the development of drugs and medical devices.
Totzke & Dreher
Medical Writing Services, Clinical and Scientific Consultancy for Regulatory Affairs, Clinical Development, Medical Communication, and Marketing
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preclinics is a partner for the development of drugs (small molecules, peptides, biologicals etc.), **** delivery formulations and medical devices.
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Locum International is a Pharmaceutical Research and Development Company specialising in **** development, scale-up, validation and regulatory affairs in the ANDA and NDA global market. Incorporates IAGIM, a **** Development Research Association publishing Scientific Generic Pharmaceutical journals and technical Handbooks Generic Dosage form Know-how and Off Patent Innovative **** Development.
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Noxopharm is an Australian publicly-listed (ASX: NOX) clinical stage **** development company. The clinical stage **** candidate is Veyonda® (previously known as NOX-66). Veyonda® is a first-in-class, dual-acting cytotoxic and immuno-oncology **** candidate designed to enhance the effectiveness and safety of both chemotherapy and radiotherapy
Professional clinical trial support | GLANIS Trusted Services
Glanis Trusted Services offers professional clinical trial support, clinical monitoring and trial management, regulatory consultancy and quality assurance.
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Veterinary Consultants - Veterinary Pharmaceutical Consultants - Vet CRO
Veterinary consultants - veterinary pharmaceutical consultants, veterinary research, veterinary **** development, veterinary clinical trials.
Cogitars - supporting innovation
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Regulatory strategies & consultancy service for medical device manufacturers | MT Promedt Consulting
MT Promedt Consulting develops regulatory strategies and delivers innovative solutions to the needs of the medical device and **** industry. Find out more!
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Preclinical toxicology consultant with CRO experience. Using years of relevant hands-on experience I give practical support to your development programme.
Cortex Discovery
AI-based **** discovery in the preclinical area. We offer services and partnership opportunities for **** development from hit discovery to lead optimization.
Dr. Matthias Brunner – Entrance
Dr. Matthias Brunner, **** Regulatory Affairs Consultant
Author: Dr Matthias Brunner
Dr. Matthias Brunner – Entrance
Dr. Matthias Brunner, **** Regulatory Affairs Consultant
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Other websites similar as preclinconsulting.ch
Home - Curis, Inc
About Curis is a biotechnology company focused on the development and commercialization of innovative therapeutics for the treatment of cancer. We currently have three **** candidates in development: Fimepinostat (formerly known as CUDC-907), an **** available, small molecule inhibitor of HDAC and PI3K enzymes being investigated in a Phase 2 clinical trial in patients with […]
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TD2, a leading oncology CRO, advances oncology research by guiding pharmaceutical and biotechnology therapies from preclinical and clinical trial phases to FDA approval.
Arkin Consulting Group, LLC.
Regulatory affairs consulting FDA ISO medical device cGMP quality assurance control audit submission NDA 510(k) IDE clinical pharmaceutical registered agent compliance recall 483
Experien Group |
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A Shanghai-based integratedNonhumanPrimateCRO and researchplatform providing disease models on key disease areas for **** efficacy or pharmacology assessment in nonclinical or preclinical phase, with human translatable endpoints.
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TRANSVAC seeks to support vaccine-related projects currently in the preclinical phase of development. TRANSVAC’s goal is to further support and accelerate vaccine-related projects by providing access to the services and expertise and to ultimatly implement a European vaccine R&D infrastructure .
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Credevo is a global consulting organization specializing in regulatory, clinical development, licensing (out-/in-), and feasibility support for pharmaceuticals, nutraceuticals, medical devices, and biologics worldwide. Credevo facilitates global regulatory submissions, and cross-regional conduct of clinical development projects, particularly in Asia-Pacific and North America regions. Through innovative online platform, Credevo facilitates clinical trial feasibility with more than 100,000 investigators around the world.
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