Enterprise Ireland Events

4 Jan Fundamentals of Technology Transfer & Advanced Licensing Skills
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2 Oct Microbiological Challenges in the Biotechnology Industry
Includes site tour of Wyeths QC and Micro Labs (places limited)Topics addressed inclued*Brief presentation on Wyeth Biotech *Design of Biopharmaceutical Facilities *Creating Efficiencies in Cleanroom Environmental Monitoring Programs*Case Study: Recovery environmental monitoring following planned/un...read more read more
27 Nov Coaching: A Mandatory Skill for 21st Century Leaders
Association for Coaching presentsEXCELLENCE IN COACHINGCoaching: A Mandatory Skill for 21st Century Leaderswith Sir John WhitmoreTuesday 27 November, 2007 - DublinDATE: Tuesday 27 November 2007 15.00 - 15.30 Registration 15.30 - 18.00 Workshop 18.00 - 18.30 NetworkingSPE...read more read more
20 Feb BioMed Central 11 2008 - Enabling Healthcare in the 21st Century
Wednesday 20 February 2008Connected health encompasses a diverse range of emerging technologies and services in healthcare. Connected health allows the development of patient-centred, personalized healthcare, and provides new opportunities for innovation and partnerships among researchers, practitio...read more read more
4 Mar Private Equity Conference Belfast
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3 Apr The Whittaker Awards 2008
[image;whittakerbanner.jpg;The Whittaker Awards] The Whittaker Awards 2008 will take place on Thursday 3rd April at John Hume Building in NUI Maynooth at 7pm. The competition is organised by the NUI Maynooth Biological Society with support from the Enterprise Ireland Lifescience & Food Commercialis...read more read more
9 Apr 9th & 10th of April 2008 - Central London - UK
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24 Apr Risk Based Management in Pharmaceutical Microbiology
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26 May 7th Training Course on High-throughput (HT) Drug Metabolism/Disposition (DM/D),
Wll be held between May 26 and May 30, 2008 in Amsterdam, The Netherlands.The EUFEPS Committee on Industrial Relations (CIR) initiated this Course, which has become self-sustaining, a clear sign of quality and success. The course is now concentrated into five full teaching days, including lectures a...read more read more
11 Nov Reporting Failure Investigations and Process Deviations
Dublin, Ireland...read more read more
1 Mar Adverse Drug Events - Reporting & Regulatory Requirements
Berlin, Germany...read more read more
24 Mar Root Cause Analysis for CAPA
Dublin, Ireland...read more read more
29 Mar Effective Quality Assurance Auditing for FDA Regulated Industries
Dublin, Ireland...read more read more
14 Apr CMC Regulatory Compliance for Biopharmaceuticals and Biologics
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15 Apr Writing Effective Standard Operating Procedures and Other Process Documents
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19 Apr QA/QC Strategy for Biopharmaceuticals and Biologics
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19 Apr cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
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22 Apr Introduction to Effective Medical Writing
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22 Apr Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
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22 Apr Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
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26 Apr FDA Inspections of Clinical Data Systems
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26 Apr The EU Clinical Trial Directive
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28 Apr European Filing & Registration Procedures
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17 May Practical Methods for Project Management
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19 May Root Cause Analysis for CAPA
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24 May Overview of FDA Regulatory Compliance for Medical Devices
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24 May Clinical Trial Design for Medical Devices
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29 Sep The Drug Development Process - From Discovery to Commercialization
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5 Oct The EU Clinical Trial Directive
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7 Oct European Filing & Registration Procedures
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11 Oct Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
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21 Oct Auditing and Qualifying Suppliers and Vendors
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30 Oct Effective Document Management for Pharmaceutical, Biotech, & Medical Device Industries
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4 Nov Stability Programs for Product Shelf Life - From Development to Approval
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4 Nov Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
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10 Nov The CTD/eCTD: Building the Marketing Application throughout Clinical Development
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4 Apr Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
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4 Apr Effective Document Management for the Pharmaceutical, Biotech & Medical Device
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4 Apr Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
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5 Apr Innovation in Separations Science
With the huge success of UPLC and MS in the Irish market this year, Waters is delighted to announce Innovation in Separations Science (ISS) 2011, a unique forum where Irish scientists will present their innovative applications of our technologies.The program consists of lectures in both basic and ad...read more read more
6 Apr QA/QC Strategy for Biologics and Biopharmaceuticals
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6 Apr cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
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7 Apr Introduction to Effective Medical Writing
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7 Apr Integrated Tablet Formulation Development
This unique 2 day course introduces and integrates the key elements of tablet development based on the principles of Quality by Design (QbD) set out in ICH Q9. It will include experimental, hands-on experience of formulation development and will cover: * The product development lifecycle* Preformul...read more read more
11 Apr Development and Validation of Bioanalytical Assays for Biologics: Quantification (PK) And Immunogenicity Assays
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11 Apr Tablet Formulation Development, Validation and the application of QbD
This interactive workshop provides up-to-date, relevant and detailed information on the impact of Quality by Design (QbD) on the Development and Validation of tablet manufacturing processes. It will also study the identification and evaluation of Critical Product Attributes and Critical Process Par...read more read more
11 Apr How to Audit API Manufacturers
This one day seminar is aimed at QA staff in drug products manufacturers and especially their QPs who have specific responsibilities under directive 2004/27/EC.QPs are required to declare that the active materials used in each of their products have been manufactured to GMP as interpreted by the EU....read more read more
13 Apr GMP Auditor Training
This 2 day course is aimed at Quality Assurance auditors and production management for Level 2 internal audits and supplier auditing.To be a business benefit rather than a drain on resources, your auditing programmes must be integral to continuous improvement. The key to effective internal auditing...read more read more
14 Apr Writing Effective Standard Operating Procedures and Other Process Documents
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5 May Supply Chain Management in Pharma/Biotech
This 2-day workshop aims to provide participants with a complete overview of professional supply chain management processes used across all sectors and then spotlight the issues and opportunities that exist specifically within pharmaceuticals.The format of the workshop will be interactive, using cas...read more read more
9 May Technology Transfer
This 2-day interactive workshop is intended to provide an overview of the challenges that must be overcome in transferring technology and to highlight some proven techniques for overcoming those challenges.Some of the benefits to be derived from this workshop include: **An appreciation of where TT f...read more read more
12 May Practical Methods for Project Management
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16 May FDA Inspections - What Regulators Expect and How to Prepare
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16 May Process Validation for Medical Devices
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16 May Stability Testing in Pharmaceutical Development and Manufacture
The purpose of this course is to give a comprehensive, integrated overview of pharmaceutical stability testing. It will include, A comprehensive review of ICH guidance, Pitfalls in stability testing, Outsourcing-costs and benefits, New approaches to stability testing including ASAP, Stability Test...read more read more
18 May Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biologics
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19 May How to Implement Risk Management Principles and Activities within a Quality Management System
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19 May Clinical Document Management - A Trial-by-Trial Approach to Compliance
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23 May Project Management for Phase 1 & 2 Clinical Trials
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25 May Project Management for the Phase 3 and LCM (Life Cycle Management)
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1 Jun FDA Inspections of Clinical Data Systems
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9 Jun Pharmacokinetics in Drug Development - an integrated approach
The object of this course is to provide participants with an overview of the principles of Pharmacokinetics and Pharmacokinetic/Pharmacodynamic modelling and how together with regulatory guidances they can be used to effectively deliver drug development programmes. Participants will gain an understa...read more read more
14 Jun Centralized Monitoring, Alarming and Reporting System Workshop
Join us for a free Seminar and learn more about the Labwatch Centralized Monitoring, Alarming and Reporting System. Venue: GE Sensing - Shannon, Ireland...read more read more
19 Sep An introduction to LC-MS for Pharma Industry
This one-day course provides an introduction to technology and (potential) application areas of combined liquid chromatography-mass spectrometry (LC-MS) in small-molecule pharmaceutical industry. The morning sessions provide a clear technology overview, introducing analyte ionization techniques, dif...read more read more
20 Sep Quantitative Bioanalysis using LC-MS
This advanced application-oriented two-day course in LC-MS pays attention to the important aspects of quantitative bioanalysis by LC-MS, except for statistical aspects in data-processing. Starting from providing knowledge on important processes in analyte ionization by electrospray or APCI, the co...read more read more
13 Oct Writing effective SOPs in a GMP environment
This course provides helpful information by presenting topics associated with the writing, formatting, execution, management and global harmonization of SOP's. It also discusses good documentation practices required by companies to ensure GMP compliance and relates the role which SOP's play in achie...read more read more
18 Oct OOS investigations in a GMP environment
This course is designed to provide essential training for conducting Out of Specification (OOS) investigations in a GMP environment. A background discussion of the associated GMP documentation required to support the OOS investigation is included but the majority of time is spent detailing the who, ...read more read more
22 Nov HPLC Analytical Method Development and Validation
Analytical methods must be validated to provide reliable data for regulatory submissions. These methods are essential for a number of purposes, including testing for QC release, testing of stability samples, testing of reference materials and to provide data to support specifications. This course pr...read more read more
30 Nov Development and Manufacture of Effervescent Tablets
About this course:Effervescent products present particular problems in manufacture, which result from their special requirements and particular utility. In this one day workshop led by two leading experts, the issues surrounding the development and manufacture of effervescent products are explored ...read more read more
14 Dec Introduction to Photostability
The purpose of this course is to give an overview of photostability,and where it fits in the stability testing programme and the importance of photostability. The course is highly interactive and held in a relaxed environment.It will cover:* Why do we do photostability tests?* Concepts and backgro...read more read more
14 Dec Pharmaceutical Packaging - an introductory course
Pharmaceutical Packaging is a very specialised area with its own unique issues and problems. This one day course will provide delegates with a good basic grounding and appreciation of what is required for the packaging of pharmaceutical and healthcare products. Whether you know nothing, have a bas...read more read more
22 Jul SBE's 4th International Conference on Bioengineering and Nanotechnology (ICBN) 22-24 July 2008, UCD, Dublin, Ireland
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4 Oct Innovation and Technologies Showcase
  Trinity College Dublin’s Technology Transfer Office will be hosting  the annual Innovation and Technologies Showcase in the O’Reilly Institute on Thursday 4th October 2012,  from 4-8pm With Trinity’s record of 27 spin-out companies in the last 5 ...read more read more
28 Nov Big Ideas Technology Showcase
  Sometimes the big ideas in med-tech innovation are about getting a better edge. Perhaps a hip replacement with tiny, directional claws on its surface that gives the implant a better grip in the recipient's thigh bone. Or 'self-cleaning' hospital uniforms, wh...read more read more