- Cancer Biology & Biomarkers
- Chromatography & Mass Spectrometry
- Contract Research, Clinical Trials and Outsourcing
- Drug Discovery
- Drug Targets
- Flow Cytometry
- Informatics & Lab Automation
- Ingredients, Excipients and Dosages
- Microbiology & RMMs
- NIR, PAT & QbD
- Raman Spectroscopy
- Screening, Assays & High-Content Analysis
- Thermal Processing
Enterprise System Partners (ESP)
Tel: 00353 21 4614400
Enterprise System Partners (ESP) is a leading global consulting and project engineering company – supporting manufacturing IT solutions for the life science industry since 2003.
We offer specialist support and consulting services exclusively for manufacturing and supply chain operations in biotechnology, pharmaceutical and medical devices, with core focus on Manufacturing Execution Systems (MES) and serialization.
Our specialist consultants and engineers have the expertise to support the concept, planning, vendor selection, design and implementation of the entire manufacturing systems landscape from process automation to the enterprise layer (level 0-4).
We have offices in Cork, Boston, Istanbul, Oss, San Francisco and the Research Triangle allowing us to support projects with local resources worldwide.
As the cost of compliance increases and pressure to achieve greater efficiency in manufacturing heightens, MES provides near real-time production data allowing optimal use of people, equipment and materials on the shop floor.
When considering MES as a solution, early assessment of your needs, planning and selecting the correct option is essential to optimize the impact of the system for your plant.
ESP has been offering its clients strategic support in the selection and implementation of MES for over a decade. As a vendor independent consultancy, we are experts in all the major MES Platforms including: Werum, Rockwell, POMs, Emerson, Siemens and Camstar
MBR Factory improves MBR build quality and reduces cost. After initial client/integrator process mapping, the specialist ESP team develops the model governed by the defined scope. The product is reviewed with full client interaction and delivered to site for a Site Acceptance Test (SAT). On successful completion, the system is handed over to the client together with required support from ESP.
- Improve MBR Build Quality
- Decrease Cost
- Optimal Use of Business Resources
- Access to Specialist MBR Modellers
- Fully Managed Project with Pre-Determined Scheduling
Serialization, the marking and tracking at unit of sale level of prescription pharmaceuticals, is a rapidly developing requirement for all major markets worldwide.
ESP has a unique blend of knowledge specialists from level 0 to level 4 and across the supply chain.
This gives us a distinct advantage in the delivery of serialization solutions.
We have worked with many of the early adopters within the life science industry, developing and executing their serialization strategies so they are internationally compliant for the future.
- 5th Traceability & DQSA Conference, New Jersey, May 10-11 2016
Manufacturers and distributors are finding themselves with their backs closer and closer to the wall in the face of the looming deadlines and requirements of the Drug Quality and Security Act (DQSA).
ExL Pharma is convening a speaking faculty of industry experts and peer groups of brand protection, supply chain management and regulatory compliance professionals to ensure success in meeting the DQSA 2017 deadline and other ominous deadlines. The 6th Traceability and the DQSA Conference will elucidate best practices; highlight lessons learned; and showcase innovative solutions for the implementation, data exchange and IT architecture for national and global serialization programs.
- MES 2016, Philadelphia, Aug 10-11 2016
MES 2016, the life science industry’s most in-depth manufacturing systems-focused event is packed with breakthrough content and next-generation strategies for achieving the highest ROI on your MES activities. Gain insight on innovative applications and processes to master this advanced IT-based solution in a highly regulated environment. Collaborate with peers and zero in on prevailing industry approaches to ensure manufacturing intelligence and excellence by successfully deploying, integrating, maintaining and utilizing data from MES.
- MES & Process Minds 2016, Berlin, Sept 29-30 2016
we.conect’s annual MES & Process Minds is gathering global players and local hidden champions of the pharmaceutical industry to explore the latest developments in the field of MES. The conference is an international knowledge exchange platform bringing together all stakeholders who play an active role in the MES scene and is the calendar event amongst MES professionals.
ISPE Boston Show, Boston, Oct 5 2016
- Serialisation & Traceability Summit, Geneva, Nov 8-9 2016
Pharma Serialisation & Traceability 2015 brought together over 130 pharma and biotech professionals gathered in Geneva for the 6th Annual Pharmaceutical Serialisation & Traceability conference. Across three days, key players and decision makers heard the latest regulatory updates from EMVO, GS1, Ministry of Health & Welfare, Republic of Korea; regulators and associations. Concepts discussed included the role of global standards in Key markets, level 4 integration, the final delegated acts and whether the industry will be left with enough time to get serialised. This November, hear EMVO, GS1, Ministry of Health & Welfare, Republic of Korea; regulators and associations give critical regulatory updates to ensure you are up to speed with the imminent deadlines.