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Aptuit is a global pharmaceutical services company that delivers early to mid-phase drug development solutions to more than 800 companies by applying scientific excellence, outstanding service and a team of some of the foremost scientific professionals in the industry. From seven locations around the world, including our strategic partner in India, Aptuit assists clients by shortening their timelines and delivering on time, in full. We solve scientific problems through technical expertise and superior project management. We provide significant value to our clients by delivering high quality services that exceed regulatory compliance standards.

Aptuit services include:
• Drug Design & Discovery
• Preclinical Biosciences
• API Development and Manufacture
• Solid State Chemistry
• Solid, Oral and Sterile Dosage Form Development and Manufacture
• Clinical Sciences
• Consulting
• Aptuit INDiGO® - Accelerated Drug Development Program
• Integrated Drug Discovery and Development

Aptuit (Glasgow) are specialist providers of formulation development and GMP manufacture of sterile dosage products, both liquid and lyophilised, for use within pre-clinical and clinical trials.

Our dedicated formulation scientists are experts in the delivery of complex formulations for liquid and lyophilised product types for small organic molecules through to large macromolecules (peptides, proteins, oligonucleotides etc). This is supported by a team of dedicated analytical scientist who are able to develop, validate or transfer analytical methods for use in the development of the formulation.

Come and see us at booth #73

Physiomics plc combines systems biology with cutting edge mathematics to develop models that streamline the drug discovery and development process. Virtual Tumour, the company’s lead service, is used to optimise the dosing and scheduling of oncology drugs in pre-clinical trials, reducing the need for animal experiments. This optimisation also improves the efficacy of combinations in pre-clinical xenografts.

The company is also developing:

(i) Virtual Tumour Clinical, to directly predict optimal regimens for human clinical trials.

(ii) Cardiac tox prediction service, to predict unwanted toxic side effects of drug candidates early on in the drug discovery process.

(iii) Drug combinations database, for researchers and clinicians to rapidly access literature data on pre-clinical and clinical regimens and their effects.

Physiomics has worked with Eli Lilly since 2007 and recently added a further two large pharmaceutical clients. In addition, Physiomics has collaborated with a number of other companies including Bayer Technology Services, Sareum, ValiRx, Cancer Research Technologies and Cyclacel. Fee-for-service, licensing and revenue sharing options are available.

Competitive Drug Development International is an international biotechnology and pharmaceutical consulting company. Unlike a traditional consultancy who talk and advise, our mode of working is hands-on and delivery focused, in addition to the strategic planning. From evidence based protocol feasibility, to management of CROs and CMOs, to delivery of POC, we can achieve your specific objectives quickly and more cost-effectively. Come and see us at Bio-Europe 2012 in Hamburg at booth #27.

Come and see us at booth #73

Diamond Pharma Services is a leading technical and scientific consulting group of companies serving the biotechnology and pharmaceutical industry. Our emphasis is on the following areas:

•    Regulatory Affairs: From Product Concept to Registration and Beyond
•    Product Development: Nonclinical, CMC and Clinical Aspects
•    Pharmacovigilance: Clinical trial (Phase I-IV), Post-Marketing and QPPV Services
•    Compliance: GLP, GMP, GCP and QP Services

Our clients range from virtual start-up companies to the largest multi-national corporations. Our expertise includes products of recombinant DNA and hybridoma technology, nucleotide based products (RNA and DNA), synthetic peptides, chemical entities (innovative and generic), vaccines (therapeutic and prophylactic), blood products and advanced therapy medicinal products (gene and cell therapy products).

We have sophisticated and well-equipped office facilities and a state-of-the-art IT system. Our IT system includes a fully validated in-house eCTD system (Extedo) and safety database (ARISg). The company was founded in 2005 by Dr. Maureen Graham, formerly Director of Regulatory Affairs at Amgen. Our specialised team of more than 27 professionals includes those with a broad and varied industry experience and former regulators, offering both breadth and depth of expertise, from which our clients can benefit.  

Contact details:

Paul Cronin
Director of Business Development
Diamond Pharma Services Limited
No 4 East Wing, Gemini House
Flex Meadow, Harlow
Essex, CM19 5TJ
United Kingdom
Tel:     +44 (0)1279 441616
Fax:     +44 (0)1279 418964
Email:    pcronin@diamondpharmaservices.com
Web:    www.diamondpharmaservices.com

Come and see us at booth #73