Quay Pharma provide a comprehensive Pharma R&D service, including the
most advanced analytical techniques. We specialise in the optimisation
of dosage forms including the design of conventional and controlled release
tablets and capsules. We operate a pilot scale manufacturing facility to
cGMP and can carry out granulation, compression, coating, capsule filling
etc. Our scientific staff have exceptional experience gained in industrial
and academic environments.
Bio-Images Research Ltd was founded in October 2000 as a spin out company from the Universities of Strathclyde and Glasgow.
Bio-Images undertakes early phase clinical studies in volunteers and patient groups, specialising in gamma scintigraphy.
This non-invasive imaging technique is used to monitor oral, gastrointestinal, nasal, pulmonary and ophthalmic systems.
We also undertake pharmacokinetic studies and our on-site analytical laboratory enables us to provide a complete service to our clients.
All studies are fully compliant with ICH-GCP guidelines with all clinical trial supplies manufactured in a GMP facility
White Rose Consultant
For succeeding, White Rose Consulting aims to work with organisations to help them achieve their objectives of scientific and
commercial excellence in their own particular fields. This promises to be a friendly yet highly effective consultancy,
with whom to entrust, with confidence, your highest priority work.
Northern Science Consulting Inc.
１． Research, development and sales of software and computer systems related to science and technology such as
genes, protein analysis, drug disposition, etc.
２． Research and consultancy services related to science and technology such as genes, protein analysis, drug disposition, etc.
３． Introduction and sales of international solutions regarding the above.
Med Discovery’s mission is the discovery and development of highly specific protein drugs to treat uro-genital cancers.
By combining biological drug discovery expertise with a strong in-house knowledge of the medical urology field, the Company
is uniquely positioned to develop novel drugs for urological cancers and other related solid tumors. Med Discovery wants
to become a worldwide leading research and development biotech company in the field of uro-genital cancer treatments.
Technology Catalysts International
Technology Catalysts International (TCI) was founded in 1979 to provide consulting services that satisfy the technology
transfer and business research needs of industry. We specialize in technology licensing, technology assessment,
and technology portfolio management. The TCI headquarters are located in Falls Church, Virginia; a suburb of Washington, DC.
Our global network also includes offices and associates in the United Kingdom, Germany, the Czech Republic, Japan, Korea, China, India, and Argentina.
EAS Consulting Group, LLC
EAS specializes in US Food and Drug Administration (FDA) regulatory matters. Our prime focus is to assist domestic and foreign pharmaceutical,
medical device, food, dietary supplement, and cosmetic firms and to comply with applicable laws and regulations. EAS is staffed with former FDA
compliance and inspection officials, and is assisted by an extensive network of consultants with many years of FDA and industry experience.
Soas has a long experience for introduction of the computer system and implementation of the Computer System Validation (CSV) for pharmaceutical industries.
Major expertise are ;
1. Introduction management consultation and support for ERP, MES, LIMS etc..
2. CSV consultation and support work for implemented system such as above.
3. Review, prepare, develop and consult the protocols and procedures relating to
Pharma Associate Co.,Ltd.
We will answer a regulation and a customer demand about Drugs, Cosmetics and Medical Devices Act-related wide
chemical products as a final usage of the chemical products. We let both a business side and a production side
reflect a different demand of each country and company efficiently, and solved it. Also we are based on the demand
of the recent authorities and he aims at the accurate correspondence to an application, change and maintenance of DMF and MF.
The CEO acquired a Master’s degree of in Pharmaceutical Chemistry in a graduate school. He was engaged in
Pharmaceutical and Bio business related work in one of the leading chemical company in Japan for more than 30 years.
During this time his roles included the following;
-The process examination & commercialization of API and Pharmaceutical
intermediate using organic synthesis, fermentation and mammalian cell culture
technology in the production site.
-The global business of the developments and sales of API and pharmaceutical intermediate in a business division.
-The administration management of the drug company of a subsidiary business division.
-Inspection correspondence with the authorities and the customers. The application of DMF(FDA),MF(PMDA) and SMF(PIC/S) in a quality assurance division..
【Qualifications】Certified Pharmacist and IRCA QMS Provisional Auditor(Competence) ISO9001:2008