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PHATOPHY

  • Pre-clinical development and testing, pre-clinical CRO
  • Human Medicines
  • Europe

Phatophy is an Independent CRO, specialized in providing high quality development services to the human and veterinary pharmaceutica/ biological companies, biotechs and academic laboratories  from proof of concept to regulatory studies throughout the whole development of your candidates, projects, products, medical devices and feed additives. Phatophy has developed expertise and excellence in different activities: • Pharmaceutical development (analytical development, quality control, stability studies) • In Life studies (pre-clinical and clinical studies) • Bio-analyses (developpment and validation) on many biological matrices (serum, plasma, tissus, urine, feaces, milk eggs,...) • Regulatory Affairs and Project Management • Quality control Phatophy is GLP (BPL) accredited by ANSES French National Agency. Phatophy has Research Tax Credit (“Crédit Impôt Recherche / CIR”) agreement for the coming years. This agreement, obtained from the French authorities, permits to the clients working with Phatophy to refund R&D expenses to their corporate taxes. Phatophy is a member of www.lyonbiopole.com network. More »

Medi-Mogul Consultancy

  • Regulatory services - CMC writing - medical writing
  • Medical Devices
  • Europe

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Voisin Consulting Life Sciences

Logo Voisin Consulting Life Sciences
  • Regulatory services - CMC writing - medical writing
  • Human Medicines
  • Europe, North America, Asia

We are a regulatory consulting company. We assist in the design and implementation of customized regulatory strategies for the innovative development and registration of healthcare products. More »

Pharmaceutical Development Group (PDG), Inc.

Logo Pharmaceutical Development Group (PDG), Inc.
  • Regulatory services - CMC writing - medical writing
  • Human Medicines
  • North America

  We assist FDA regulated firms in the navigation of the U.S. submission and approval procedures across a variety of dosage forms and therapeutic areas.  Our expertise spans prescription and non-prescription (OTC) drugs, biologics and medical devices.  we are supported by our full time professional staff and consultants including pharmacologists, epidemiologists, toxicologists, clinicians, analytical scientists, regulatory strategists, business development administrators, labeling experts and others.  With extensive combined experience in securing FDA approvals, we are well versed in strategic product planning and regulatory consulting. More »

Salzman Capital Ventures

  • Pre-clinical development and testing, pre-clinical CRO
  • Human Medicines
  • North America

Salzman Capital Ventures, Ltd. (SCV) provides full-service pharmaceutical support, including custom laboratory R&D operations, and drug development consultation.   Our reputation has been built on the most technically demanding projects, typically directed at new biological targets and innovative pharmacologic interventions. More »

Dr Rubina Mushtaq - Freelancer

  • Regulatory services - CMC writing - medical writing
  • Human Medicines
  • Africa

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Explora Laboratories SA

Logo Explora Laboratories SA
  • Contract manufacturing, filling and packaging
  • Biopharmaceuticals
  • Europe

EXPLORA LABORATORIES SA provides to its customers a platform of services, ranging from Research and Development at laboratory scale to commercial supply of active pharmaceutical ingredients and key intermediates. More »

Clinstat GmbH

  • Quality management services
  • Human Medicines
  • Europe

ClinStat is an independent contract research organization (CRO) in Cologne, Germany. Since our foundation, we supported in particular pharmaceutical companies, hospital facilities, manufacturers of medicinal products as well health insurance providers and other medically-oriented institutions. We offer services for pre-clinical studies, phase I-IV clinical studies, post-marketing studies and meta-analyses in pharmaceutical research. Additionally, we are an experienced partner for epidemiological studies, studies in health services research/public health as well as studies concerning health economics. The cornerstone of success at ClinStat is our excellent team, which has a broad scientific background and profound knowledge in its field. Together, we work according to international quality standards and guidelines. Thereby, we also have the competence and capability to consider the client-specific needs. We look forward to working with you and consider your success as our mission. More »

Nia Life Sciences

Logo Nia Life Sciences
  • Pre-clinical development and testing, pre-clinical CRO
  • Biopharmaceuticals
  • North America

Welcome to Nia Life Sciences, Inc., a Preclinical Research Facility Servicing Biotech and Pharmaceutical Industries. Nia Life Sciences, Inc. is a contract research organization (CRO), located in Libertyville, IL. We provide services for conducting toxicology, pharmacokinetics and metabolism studies. Our studies in rodents are performed in full compliance with Good Laboratory Practice (GLP) regulations. All protocols are designed to meet client's needs and the regulatory requirements. We adhere to the regulations and guidelines for Animal Care and Welfare. More »

ToxPharm Consulting

Logo ToxPharm Consulting
  • Regulatory services - CMC writing - medical writing
  • Biopharmaceuticals
  • North America

An independent consulting company providing scientific and regulatory guidance in the areas of: Toxicology and Pharmacokinetics Regulatory Strategy and Safety Assessment Regulatory Submissions and Negotiations Study Design, Monitoring, Compliance, Reporting Licensing and Acquisitions of Drug Development Candidates   More »

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