Consulting, Training and Other Pharmaceutical Services
| A-consult | ||
A-consult provides professional regulatory affairs services that help pharmaceutical companies gain marketing authorisation for medicinal products. |
A-consult provides tailor-made pharmacovigilance and drug safety services to ensure that products comply with increasing safety requirements. |
A-consult offers professional assistance to the pharmaceutical industry within all areas of regulatory affairs and drug safety. |
| DBA | ||
DBA offers a comprehensive range of courses to meet your needs, from Qualified Person (QP) training and our new Quality Leadership Program in the US, to residential and in-house pharmaceutical training. |
DBA provides training to aspiring Qualified Persons in collaboration with the University of Strathclyde. |
Our Quality Leadership Program sets new standards for practical, results-oriented instruction. |
Our pharmaceutical training, consultancy and auditing services maximise the effectiveness of your teams globally. |
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| ERG (Air Pollution Control) | ||
A V-tex scrubber unit installed at a pharmaceutical research facility for vent gas scrubbing. |
An ERG skid-mounted pilot unit in use at a major chemical facility. |
Schematic detail of a two-stage V-tex™ scrubber. |
An odour dispersion model showing atmospheric dispersion from a proposed new process plant. |
An ERG odour control unit at a major waste processing facility. |
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| ESS | ||
ESS provides pharmaceutical asset maintenance consultancy services, which can improve profitability and ensure long-term competitiveness. |
Our pharmaceutical asset management training courses are designed to be interactive; they offer professionals the chance to network. |
Our resource outsourcing service allows us to provide interim or permanent managers and technicians quickly and cost-effectively. |
Continuous maintenance improvement and condition-based maintenance enable pharmaceutical companies to reduce cost and maintain efficiency. |
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| Global Vision | ||
Digital-Page, an artwork verification tool, helps eliminate artwork errors by comparing files for differences. |
Global Vision’s artwork inspection systems detect all changes including color, missing or added text, and barcode and registration errors. |
Docu-Proof, a text verification and document comparison tool, inspects packaging and critical documents for errors regardless of format or layout. |
Docu-Proof is a text verification and document comparison tool that compares text in any language, including Braille, to avoid the implications of a dropped character on a label or packaging component. |
Global Vision’s electronic label inspection, text verification and document comparison solutions ensure all documents and artwork remain error free throughout the pharmaceutical packaging process. |
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| ICD Research | ||
The Industry Outlook report series reveals how buyer's procurement and business needs and supplier's marketing practices are changing. |
Sample page 1 |
Sample page 2. |
| PharmaLex International | ||
PharmaLex International provides specialized support for worldwide drug registrations, enabling rapid and uncomplicated registration. |
Optimize your resources with PharmaLex's expertise in all regulatory affairs issues - let PharmaLex free your mind. |
During the drug registration process PharmaLex deals with the preparation and submission of the dossier, the supervision of the official registration process, communication with the authorities and translation of product texts into local languages. |
Today PharmaLex is one of the largest companies offering worldwide drug registration services, and has successfully compiled registration dossiers in more than 100 countries. |
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| Somerset House Consultants | ||
Managing Director Robert Haslam has over 30 year's experience in pharmaceutical development, manufacturing, quality assurance, validation and regulatory affairs. |
All work is carried out in compliance with current EU, FDA and ICH Good Manufacturing Practice. |
Somerset House Consultants is experienced in the manufacture and QP release of clinical trial supplies (IMP) in accordance with directive 2001/20/EC. |
